DC-3/DC-3T DIAGNOSTIC ULTRASOUND SYSTEM

K083505 · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · IYN · Dec 12, 2008 · Radiology

Device Facts

Record IDK083505
Device NameDC-3/DC-3T DIAGNOSTIC ULTRASOUND SYSTEM
ApplicantShenzhen Mindray Bio-Medical Electronics Co., Ltd.
Product CodeIYN · Radiology
Decision DateDec 12, 2008
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 892.1550
Device ClassClass 2
AttributesPediatric, 3rd-Party Reviewed

Intended Use

The device is intended for use by a qualified physician for ultrasound evaluation of abdominal, cardiac, small parts (breast, testes, thyroid, etc.), peripheral vascular, fetal, transrectal, transvaginal, intraoperative (abdominal, thoracic, and vascular etc. ), pediatric, neonatal cephalic, musculoskeletal (general and superficial).

Device Story

Mobile, software-controlled diagnostic ultrasound system; acquires/displays images in B-Mode, M-Mode, Color, PW, CW, Power, DirPower, and combined modes. Employs linear, convex, and phased array probes (2.0–12.0 MHz). Used in clinical settings by physicians for diagnostic evaluation. System processes acoustic signals to generate real-time images; supports advanced features including Tissue Harmonic Imaging, Smart3D, iScape, and iBeam. Output displayed on system monitor for clinical assessment; aids in diagnosis and patient management.

Clinical Evidence

Bench testing only. Acoustic output measured per NEMA UD 2:2004 and NEMA UD 3:2004. Conformance to IEC 60601-1, IEC 60601-1-1, IEC 60601-1-2, IEC 60601-2-37, and ISO 10993-1 standards verified.

Technological Characteristics

Mobile ultrasound system; linear, convex, phased array transducers (2.0–12.0 MHz). Modes: B, M, PW, CW, Color, Power, DirPower. Features: Tissue Harmonic Imaging, Smart3D, iScape, iBeam. Safety standards: IEC 60601-1, IEC 60601-1-2, IEC 60601-2-37, ISO 10993-1. NEMA UD 2/UD 3 compliant.

Indications for Use

Indicated for ultrasound imaging in abdominal, cardiac, small parts (breast, testes, thyroid), peripheral vascular, fetal, transrectal, transvaginal, intraoperative (abdominal, thoracic, vascular), pediatric, neonatal cephalic, and musculoskeletal (general/superficial) applications. Used by qualified physicians.

Regulatory Classification

Identification

An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

Predicate Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ ## DEC 1 2 2008 # 510(K) SUMMARY This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR §807.92(c). The assigned 510(k) number is: צורך 3 לס ל ## 1. Submitter: Shenzhen Mindray Bio-medical Electronics Co., LTD Mindray Building, Keji 12th Road South, Hi-tech Industrial Park, Nanshan, Shenzhen, 518057, P. R. China Tel: +86 755 2658 2888 Fax: +86 755 2658 2680 ## Contact Person: Tan Chuanbin Shenzhen Mindray Bio-medical Electronics Co., LTD Mindray Building, Keji 12th Road South, Hi-tech Industrial Park, Nanshan, Shenzhen, 518057, P. R. China Date Prepared: October 24, 2008 ## 2. Device Name: DC-3/DC-3T Diagnostic Ultrasound System #### Classification Regulatory Class: II Review Category: Tier II 21 CFR 892.1550 Ultrasonic Pulsed Doppler Imaging System (90-IYN) 21 CFR 892.1560 Ultrasonic Pulsed Echo Imaging System (90-IYO) 21 CFR 892.1570 Diagnostic Ultrasound Transducer (90-ITX) ## 3. Marketed Device: The subject device is substantially equivalent in its technologies and functionality to the original DC-3/DC-3T Diagnostic Ultrasound System that is already cleared under premarket notification number K081320, and the other predicate devices are listed below: Mindray M5 (K083001), Mindray DC-6 (K072164). 0042 {1}------------------------------------------------ ## 4. Device Description: The DC-3/DC-3T Diagnostic Ultrasound System is a general purpose, mobile, software controlled, ultrasound diagnostic system. Its function is to acquire and display ultrasound images in B-Mode, M-Mode, Color mode, PW mode, CW mode, Power mode, DirPower mode or the combined mode (i.e. B/M Mode). This system is a Track 3 device that employs an array of probes that include linear array, convex array and phased array with a frequency range of approximately 2.0 MHz to 12.0 MHz. #### 5. Intended Use: The device is intended for use by a qualified physician for ultrasound evaluation of abdominal, cardiac, small parts (breast, testes, thyroid, etc.), peripheral vascular, fetal, transrectal, transvaginal, intraoperative (abdominal, thoracic, and vascular etc. ), pediatric, neonatal cephalic, musculoskeletal (general and superficial). ## 6. Safety Considerations: The DC-3/DC-3T Diagnostic Ultrasound System has been tested as Track 3 Device per the FDA Guidance document "Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound Systems and Transducers" issued in September 2008. The acoustic output is measured and calculated per NEMA UD 2 Acoustic Output Measurement Standard for Diagnostic Ultrasound Equipment: 2004 and NEMA UD 3 Output Display Standard: 2004. The device conforms to applicable medical device safety standards, such as IEC 60601-1, IEC 60601-1-1, IEC 60601-1-2, IEC 60601-2-37 and ISO 10993-1. #### Conclusion: The conclusions drawn from testing of the DC-3/DC-3T Diagnostic Ultrasound System demonstrate that the device is as safe and effective as the legally marketed predicate devices. 0043 {2}------------------------------------------------ Image /page/2/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with its wings spread, and the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" are arranged in a circle around the eagle. The eagle is black, and the text is also black. The logo is simple and recognizable. ## DEPARTMENT OF HEALTH & HUMAN SERVICES Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. % Mr. Robert Mosenkis President CITECH, Medical Device Testing and Consulting 5200 Butler Pike Plymouth Meeting, PA 19462-1298 DEC 1 2 2008 Re: K083505 Trade/Device Name: DC-3/DC-3T Diagnostic Ultrasound System Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: II Product Code: TYN, IYO, and ITX Dated: November 25, 2008 Received: November 26, 2008 #### Dear Mr. Mosenkis: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. This determination of substantial equivalence applies to the following transducers intended for use with the DC-3/DC-3T Diagnostic Ultrasound System, as described in your premarket notification: ## Transducer Model Number | 6CV1 | 10L4 | 3C1 | |------|------|------| | 3C5A | 6C2 | 2P2 | | 7L4A | 6LE7 | 7L5 | | 7L6 | 6LB7 | 7LT4 | {3}------------------------------------------------ If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus permits your device to proceed to market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain ) other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrb/industry/support/index.html If you have any questions regarding the content of this letter, please contact Andrew Kang, M.D. at (240) 276-3666. Sincerely yours, Joyce M. Whang, Ph.D. Acting Director, Division of Re Acting Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure(s) {4}------------------------------------------------ × #### Diagnostic Ultrasound Indications for Use Form Model: System Transducer DC-3/DC-3T 083505 510(k) Number(s) | | Mode of Operation | | | | | | | | |---------------------------------------------------------------------------------------------------|-------------------|---|-----|-----|------------------|----------------------|-----------------------|-----------------| | Clinical Application | B | M | PWD | CWD | Color<br>Doppler | Amplitude<br>Doppler | Combined<br>(specify) | Other (specify) | | Ophthalmic | | | | | | | | | | Fetal | P | P | P | | P | P | P | Note 1, 2, 3, 4 | | Abdominal | P | P | P | N | P | P | P | Note 1, 2, 3, 4 | | Intraoperative<br>(specify)* | N | N | N | N | N | N | N | Note 2, 3, 4 | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | P | P | P | N | P | P | P | Note 1, 2, 3, 4 | | Small organ(specify) ** | P | P | P | | P | P | P | Note 2, 3, 4 | | Neonatal Cephalic | P | P | P | N | P | P | P | Note 1, 2, 3, 4 | | Adult Cephalic | N | N | N | N | N | N | N | Note 1,2, 3 | | Trans-rectal | P | P | P | | P | P | P | Note 2, 3, 4 | | Trans-vaginal | P | P | P | | P | P | P | Note 2, 3 | | Trans-urethral | | | | | | | | | | Trans-esoph.(non-<br>Card.) | | | | | | | | | | Musculo-skeletal<br>Conventional | P | P | P | | P | P | P | Note 2, 3, 4 | | Musculo-skeletal<br>Superficial | P | P | P | | P | P | P | Note 2, 3, 4 | | Intravascular | | | | | | | | | | Cardiac Adult | N | N | N | N | N | N | N | Note1,2, 3 | | Cardiac Pediatric | N | N | N | N | N | N | N | Note1,2, 3 | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph.(Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | P | P | P | | P | P | P | Note1, 2, 3, 4 | | Other (specify) *** | P | P | P | | P | P | P | Note1, 2, 3, 4 | | N=new indication; P=previously cleared by FDA; E=added under Appendix E | | | | | | | | | | Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+B, Power + PW +B, | | | | | | | | | | * Intraoperative includes abdominal, thoracic, and vascular etc. | | | | | | | | | | ** Small organ-breast, thyroid, testes, etc. | | | | | | | | | *** Other use includes Urology. Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents, Note 2: Smart3D Note 3: iScape Note 4: iBeam (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(ODE) Prescription USE (Per 21 CFR 801.109) Hubert Lee {5}------------------------------------------------ | System | | | | Transducer | | X | | | |----------------------------------------------------------------------------------------------------|-------------------|---|---------|------------|---------------|-------------------|--------------------|-----------------| | Model: | | | 6CV1 | | | | | | | 510(k) Number(s) | | | K083505 | | | | | | | | | | | | | | | | | | Mode of Operation | | | | | | | | | Clinical Application | B | M | PWD | CWD | Color Doppler | Amplitude Doppler | Combined (specify) | Other (specify) | | Ophthalmic | | | | | | | | | | Fetal | P | P | P | | P | P | P | Note 2, 3 | | Abdominal | | | | | | | | | | Intraoperative (specify)* | | | | | | | | | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | | | | | | | | | | Small organ(specify) ** | | | | | | | | | | Neonatal Cephalic | | | | | | | | | | Adult Cephalic | | | | | | | | | | Trans-rectal | P | P | P | | P | P | P | Note 2, 3 | | Trans-vaginal | P | P | P | | P | P | P | Note 2, 3 | | Trans-urethral | | | | | | | | | | Trans-esoph.(non-Card.) | | | | | | | | | | Musculo-skeletal Conventional | | | | | | | | | | Musculo-skeletal Superficial | | | | | | | | | | Intravascular | | | | | | | | | | Cardiac Adult | | | | | | | | | | Cardiac Pediatric | | | | | | | | | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph. (Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | | | | | | | | | | Other (specify) *** | P | P | P | | P | P | P | Note 2, 3 | | N=new indication; P=previously cleared by FDA; E=added under Appendix E | | | | | | | | | | Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+ B, Power + PW +B, | | | | | | | | | | * Intraoperative includes abdominal, thoracic, and vascular etc. | | | | | | | | | | ** Small organ-breast, thyroid, testes, etc. | | | | | | | | | | *** Other use includes Urology. | | | | | | | | | | Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. | | | | | | | | | | Note 2: Smart3D | | | | | | | | | | Note 3: iScape | | | | | | | | | | Note 4: iBeam | | | | | | | | | (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(ODE) (Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices 510(k) Number K083505 {6}------------------------------------------------ Transducer × System Model: 510(k) Number(s) 3C5A K083505 | | Mode of Operation | | | | | | | | |-------------------------------|-------------------|---|-----|-----|------------------|----------------------|-----------------------|-----------------| | Clinical Application | B | M | PWD | CWD | Color<br>Doppler | Amplitude<br>Doppler | Combined<br>(specify) | Other (specify) | | Ophthalmic | | | | | | | | | | Petal | P | P | P | | P | P | P | Note 1, 2, 3 | | Abdominal | P | P | P | | P | P | P | Note 1, 2, 3 | | Intraoperative (specify)* | | | | | | | | | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | P | P | P | | P | P | P | Note 1, 2, 3 | | Small organ(specify)** | | | | | | | | | | Neonatal Cephalic | | | | | | | | | | Adult Cephalic | | | | | | | | | | Trans-rectal | | | | | | | | | | Trans-vaginal | | | | | | | | | | Trans-urethral | | | | | | | | | | Trans-esoph.(non-Card.) | | | | | | | | | | Musculo-skeletal Conventional | | | | | | | | | | Musculo-skeletal Superficial | | | | | | | | | | Intravascular | | | | | | | | | | Cardiac Adult | | | | | | | | | | Cardiac Pediatric | | | | | | | | | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph. (Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | N | N | N | | N | N | N | Note 1, 2, 3 | | Other (specify)*** | N | N | N | | N | N | N | Note 1, 2, 3 | Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+ B, Power + PW +B. *Intraoperative includes abdominal, thoracic, and vascular etc. ** Small organ-breast, thyroid, testes, etc. ***Other use includes Urology. Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. Nete 2: Smart3D Note 3: iScape Note 4: iBeam (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(DDE) Prescription USE (Per 21 CFR 801.109) Skelut Keun {7}------------------------------------------------ System Model: Transducer × 510(k) Number(s) 083505 7L4A | | Mode of Operation | | | | | | | | | |----------------------------------------------------------------------------------------------------|-------------------|---|-----|-----|------------------|----------------------|-----------------------|-----------------|--| | Clinical Application | B | M | PWD | CWD | Color<br>Doppler | Amplitude<br>Doppler | Combined<br>(specify) | Other (specify) | | | Ophthalmic | | | | | | | | | | | Fetal | | | | | | | | | | | Abdominal | N | N | N | | N | N | N | Note 2, 3, 4 | | | Intraoperative (specify)* | | | | | | | | | | | Intraoperative (Neuro) | | | | | | | | | | | Laparoscopic | | | | | | | | | | | Pediatric | N | N | N | | N | N | N | Note 2, 3, 4 | | | Small organ(specify)** | P | P | P | | P | P | P | Note 2, 3, 4 | | | Neonatal Cephalic | P | P | P | | P | P | P | Note 2, 3, 4 | | | Adult Cephalic | | | | | | | | | | | Trans-rectal | | | | | | | | | | | Trans-vaginal | | | | | | | | | | | Trans-urethral | | | | | | | | | | | Trans-esoph. (non-Card.) | | | | | | | | | | | Musculo-skeletal Conventional | P | P | P | | P | P | P | Note 2, 3, 4 | | | Musculo-skeletal Superficial | P | P | P | | P | P | P | Note 2, 3, 4 | | | Intravascular | | | | | | | | | | | Cardiac Adult | | | | | | | | | | | Cardiac Pediatric | | | | | | | | | | | Intravascular (Cardiac) | | | | | | | | | | | Trans-esoph (Cardiac) | | | | | | | | | | | Intra-Cardiac | | | | | | | | | | | Peripheral Vascular | P | P | P | | P | P | P | Note 2, 3, 4 | | | Other (specify) *** | | | | | | | | | | | N=new indication; P=previously cleared by FDA; E=added under Appendix E | | | | | | | | | | | Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+ B, Power + PW +B. | | | | | | | | | | | * Intraoperative includes abdominal, thoracic, and vascular etc. | | | | | | | | | | | ** Small organ-breast, thyroid, testes, etc. | | | | | | | | | | | *** Other use includes Urology. | | | | | | | | | | | Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. | | | | | | | | | | | Note 2: Smart3D | | | | | | | | | | | Note 3: iScape | | | | | | | | | | | Note 4: iBeam | | | | | | | | | | | | | | | | | | | | | (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(ODE) Prescription USE (Per 21 CFR 801.109) Herbert Lewis {8}------------------------------------------------ | System | | |------------------|---------| | Model: | 7L6 | | 510(k) Number(s) | K083505 | | Transducer | X | |------------|---| |------------|---| | Clinical Application | Mode of Operation | | | | | | | | |-------------------------------|-------------------|---|-----|-----|---------------|-------------------|--------------------|-----------------| | | B | M | PWD | CWD | Color Doppler | Amplitude Doppler | Combined (specify) | Other (specify) | | Ophthalmic | | | | | | | | | | Fetal | | | | | | | | | | Abdominal | N | N | N | | N | N | N | Note 2, 3, 4 | | Intraoperative (specify)* | | | | | | | | | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | N | N | N | | N | N | N | Note 2, 3, 4 | | Small organ(specify) ** | P | P | P | | P | P | P | Note 2, 3, 4 | | Neonatal Cephalic | P | P | P | | P | P | P | Note 2, 3, 4 | | Adult Cephalic | | | | | | | | | | Trans-rectal | | | | | | | | | | Trans-vaginal | | | | | | | | | | Trans-urethral | | | | | | | | | | Trans-esoph. (non-Card.) | | | | | | | | | | Musculo-skeletal Conventional | P | P | P | | P | P | P | Note 2, 3, 4 | | Musculo-skeletal Superficial | P | P | P | | P | P | P | Note 2, 3, 4 | | Intravascular | | | | | | | | | | Cardiac Adult | | | | | | | | | | Cardiac Pediatric | | | | | | | | | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph. (Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | P | P | P | | P | P | P | Note 2, 3, 4 | | Other (specify) *** | | | | | | | | Note 2, 3, 4 | N=new indication; P=previously cleared by FDA; E=added under Appendix E Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+B, Power + PW +B. * Intraoperative includes abdominal, thoracic, and vascular etc. ** Small organ-breast, thyroid, testes, etc. *** Other use includes Urology: Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. Note 2: Smart3D Note 3: iScape Note 4: iBeam (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(ODE) Prescription USE (Per 21 CFR 801.109) Helen Burns {9}------------------------------------------------ **Diagnostic Ultrasound Indications for Use Form**10L4 <083505 System Model: Transducer × 510(k) Number(s) | Clinical Application | Mode of Operation | | | | | | | Other (specify) | |----------------------------------------------------------------------------------------------------|-------------------|---|-----|-----|---------------|-------------------|--------------------|-----------------| | | B | M | PWD | CWD | Color Doppler | Amplitude Doppler | Combined (specify) | | | Ophthalmic | | | | | | | | | | Fetal | | | | | | | | | | Abdominal | N | N | N | | N | N | N | | | Intraoperative (specify)* | | | | | | | | Note 2, 3, 4 | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | N | N | N | | N | N | N | Note 2, 3, 4 | | Small organ(specify) ** | P | P | P | | P | P | P | Note 2, 3, 4 | | Neonatal Cephalic | P | P | P | | P | P | P | Note 2, 3, 4 | | Adult Cephalic | | | | | | | | Note 2, 3, 4 | | Trans-rectal | | | | | | | | | | Trans-vaginal | | | | | | | | | | Trans-urethral | | | | | | | | | | Trans-esoph.(non-Card.) | | | | | | | | | | Musculo-skeletal Conventional | P | P | P | | P | P | P | Note 2, 3, 4 | | Musculo-skeletal Superficial | P | P | P | | P | P | P | Note 2, 3, 4 | | Intravascular | | | | | | | | | | Cardiac Adult | | | | | | | | | | Cardiac Pediatric | | | | | | | | | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph.(Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | P | P | P | | P | P | P | Note 2, 3, 4 | | Other (specify)*** | P | P | P | | P | P | P | Note 2, 3, 4 | | N=new indication; P=previously cleared by FDA; E=added under Appendix E | | | | | | | | | | Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+ B, Power + PW +B, | | | | | | | | | | * Intraoperative includes abdominal, thoracic, and vascular etc. | | | | | | | | | | ** Small organ-breast, thyroid, testes, etc. | | | | | | | | | | *** Other use includes Urology. | | | | | | | | | | Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. | | | | | | | | | | Note 2: Smart3D | | | | | | | | | | Note 3: iScape | | | | | | | | | (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(ODE) Prescription USE (Per 21 CFR 801.109) unt {10}------------------------------------------------ × System Model: Transducer 6C22 083505 510(k) Number(s). | | | Mode of Operation | | | | | | | |-------------------------------------------------------------------------|---|-------------------|-----|-----|------------------|----------------------|-----------------------|-----------------| | Clinical Application | B | M | PWD | CWD | Color<br>Doppler | Amplitude<br>Doppler | Combined<br>(specify) | Other (specify) | | Ophthalmic | | | | | | | | | | Fetal | | | | | | | | | | Abdominal | N | N | N | | N | N | N | Note 2, 3 | | Intraoperative (specify)* | | | | | | | | | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | N | N | N | | N | N | N | Note 2, 3 | | Small organ(specify) ** | | | | | | | | | | Neonatal Cephalic | N | N | N | | N | N | N | Note 2, 3 | | Adult Cephalic | N | N | N | | N | N | N | Note 2, 3 | | Trans-rectal | | | | | | | | | | Trans-vaginal | | | | | | | | | | Trans-urethral | | | | | | | | | | Trans-esoph.(non-Card.) | | | | | | | | | | Musculo-skeletal Conventional | | | | | | | | | | Musculo-skeletal Superficial | | | | | | | | | | Intravascular | | | | | | | | | | Cardiac Adult | N | N | N | | N | N | N | Note 2, 3 | | Cardiac Pediatric | N | N | N | | N | N | N | Note 2, 3 | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph.(Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | | | | | | | | | | Other (specify) *** | N | N | N | | N | N | N | Note 2, 3 | | N=new indication; P=previously cleared by FDA; E=added under Appendix E | | | | | | | | | Additional comments:Combined modes: B+M, PW+B, Color + B, PW +Color+ B, PW +Color+ B, Power + PW +B. * Intraoperative includes sodominal, thoracic, and vascular etc. ** Small organ-breast, thyroid, testes, etc. ***Other use includes Urology. Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. Note 2: Smart3D Note 3: iScape Note 4: iBeam (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(ODE) Prescription USE (Per 21 CFR 801.109) Holt Rem {11}------------------------------------------------ × System Model: 510(k) Number(s) Transducer 6LE7 Kat3505 | | | | | | | Mode of Operation | | | |-------------------------------|---|---|-----|-----|---------------|-------------------|--------------------|-----------------| | Clinical Application | B | M | PWD | CWD | Color Doppler | Amplitude Doppler | Combined (specify) | Other (specify) | | Ophthalmic | | | | | | | | | | Fetal | N | N | N | | N | N | N | Note 2, 3, 4 | | Abdominal | | | | | | | | | | Intraoperative (specify)* | | | | | | | | | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | | | | | | | | | | Small organ(specify)** | | | | | | | | | | Neonatal Cephalic | | | | | | | | | | Adult Cephalic | | | | | | | | | | Trans-rectal | N | N | N | | N | N | N | Note 2, 3, 4 | | Trans-vaginal | | | | | | | | | | Trans-urethral | | | | | | | | | | Trans-esoph.(non-Card.) | | | | | | | | | | Musculo-skeletal Conventional | | | | | | | | | | Musculo-skeletal Superficial | | | | | | | | | | Intravascular | | | | | | | | | | Cardiac Adult | | | | | | | | | | Cardiac Pediatric | | | | | | | | | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph. (Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | | | | | | | | | | Other (specify)*** | N | N | N | | N | N | N | Note2, 3, 4 | N=new indication; P=previously cleared by FDA; E=added under Appendix E Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+ B, Power + PW +B. * Intraoperative includes abdominal, thoracic, and vascular etc. ** Small organ-breast, thyroid, testes, etc, *** Other use includes Urology. Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. Note 2: Smart3D Note 3: iScape(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(OD) Prescription USE (Per 21 CFR 801.109) Note 4: iBeam (Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices K083505 510(k) Number {12}------------------------------------------------ | System | | |------------------|---------| | Model: | 6LB7 | | 510(k) Number(s) | K083505 | | Transducer | X | | Clinical Application | B | M | PWD | CWD | Color Doppler | Amplitude Doppler | Combined (specify) | Other (specify) | |-------------------------------|---|---|-----|-----|---------------|-------------------|--------------------|-----------------| | Ophthalmic | | | | | | | | | | Fetal | | | | | | | | | | Abdominal | | | | | | | | | | Intraoperative (specify)* | | | | | | | | | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | | | | | | | | | | Small organ(specify)** | | | | | | | | | | Neonatal Cephalic | | | | | | | | | | Adult Cephalic | | | | | | | | | | Trans-rectal | N | N | N | | N | N | N | Note 2, 3, 4 | | Trans-vaginal | | | | | | | | | | Trans-urethral | | | | | | | | | | Trans-esoph.(non-Card.) | | | | | | | | | | Musculo-skeletal Conventional | | | | | | | | | | Musculo-skeletal Superficial | | | | | | | | | | Intravascular | | | | | | | | | | Cardiac Adult | | | | | | | | | | Cardiac Pediatric | | | | | | | | | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph.(Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | | | | | | | | | | Other (specify)*** | N | N | N | | N | N | N | Note2, 3, 4 | N=new indication; P=previously cleared by FDA; E=added under Appendix E Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+ B, Power + PW +B. *Intraoperative includes abdominal, thoracic, and vascular etc. **Small organ-breast, thyroid, testes, etc. ***Other use includes Urology. Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. Note 2: Smart3D Note 3: iScape Note 4: iBeam(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(OD)E) Prescription USE (Per 21 CFR 801.109) 1 (Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices, 510(k) Number K083505 {13}------------------------------------------------ Transducer × System 3C1 Model: Kod3505 510(k) Number(s) Mode of Operation Clinical Application Color Amplitude Combined PW B CWD M Other (specify) D Doppler Doppler (specify) Ophthalmic Fetal Abdominal N N N N Note 1, 2, 3 N N Intraoperative (specify)* Intraoperative (Neuro) Laparoscopic Pediatric N N N . N ਮ N Note 1, 2, 3 Small organ(specify)** Neonatal Cephalic Adult Cephalic Trans-rectal Trans-vaginal Trans-urethral Trans-esoph. (non-Card.) Musculo-skeletal Conventional Musculo-skeletal Superficial Intravascular Cardiac Adult N N Note 1, 2, 3 N N N N Note 1, 2, 3 N N Cardiac Pediatric N N N N Intravascular (Cardiac) Trans-esoph. (Cardiac) Intra-Cardiac Peripheral Vascular Other (specify) *** Nenew indication: P=previously cleared by FDA; E=added under Appendix E Additional comments: Combined modes: B+M, PW+B, Color + B, PW +Color+ B, PW +Color+ B, Power + PW+B, * Intraoperative includes abdominal, thoracic, and vascular etc. ** Small organ-breast, thyroid, testes, etc. *** Other use includes Urology. Note I: Tissue Harmonic Imaging. The feature does not use contrast agents. Note 2: Smart3D Note 3: iScape Note 4: iBeam (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(OD) (Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices 510(k) Number K083505 {14}------------------------------------------------ Transducer × System Model: . 510(k) Number(s) . ానాలు, 2P2 Kof3505 | Clinical Application | Mode of Operation | | | | | | | | |----------------------------------------------------------------------------------------------------|-------------------|---|---------|-----|------------------|----------------------|-----------------------|-----------------| | | B | M | PW<br>D | CWD | Color<br>Doppler | Amplitude<br>Doppler | Combined<br>(specify) | Other (specify) | | Ophthalmic | | | | | | | | | | Fetal | | | | | | | | | | Abdominal | N | N | N | N | N | N | N | Note 1, 2 | | Intraoperative (specify)* | | | | | | | | | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | N | N | N | N | N | N | N | Note 1, 2 | | Small organ(specify)** | | | | | | | | | | Neonatal Cephalic | N | N | N | N | N | N | N | Note 1, 2 | | Adult Cephalic | N | N | N | N | N | N | N | Note 1, 2 | | Trans-rectal | | | | | | | | | | Trans-vaginal | | | | | | | | | | Trans-urethral | | | | | | | | | | Trans-esoph.(non-Card.) | | | | | | | | | | Musculo-skeletal Conventional | | | | | | | | | | Musculo-skeletal Superficial | | | | | | | | | | Intravascular | | | | | | | | | | Cardiac Adult | N | N | N | N | N | N | N | Note 1, 2 | | Cardiac Pediatric | N | N | N | N | N | N | N | Note 1, 2 | | Intravascular (Cardiac) | | | | | | | | | | Trans-esoph. (Cardiac) | | | | | | | | | | Intra-Cardiac | | | | | | | | | | Peripheral Vascular | | | | | | | | | | Other (specify) *** | | | | | | | | | | N=new indication; P=previously cleared by FDA; E=added under Appendix E | | | | | | | | | | Additional comments: Combined modes: B+M, PW+B, Color + B, Power + B, PW +Color+ B, Power + PW +B. | | | | | | | | | | * Intraoperative includes abdominal, thoracic, and vascular etc. | | | | | | | | | | ** Small organ-breast, thyroid, testes, etc. | | | | | | | | | | ***Other use includes Urology. | | | | | | | | | | Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. | | | | | | | | | | Note 2: Smart3D | | | | | | | | | | Note 3: iScape | | | | | | | | | | Note 4: iBeam | | | | | | | | | (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(DDE) Halal Leee (Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices 510(k) Number {15}------------------------------------------------ System Transducer × Model: 7L5 510(k) Number(s) 5083505 Mode of Operation Clinical Application Color Amplitude Combined B M PWD CWD Other (specify) Doppier Doppler (specify) Ophthalmic Fetal Abdominal א ਮ N N N N Note 2, 3, 4 Intraoperative (specify)* Intraoperative (Neuro) Laparoscopic Pediatric N N N N N N Note 2, 3, 4 Small organ(specify) ** N N N N N Note 2, 3, 4 N Neonatal Cephalic ਨ N N N N N Note 2, 3, 4 Adult Cephalic Trans-rectal Trans-vaginal Trans-urcthral Trans-esoph.(non-Card.) Musculo-skeletal Conventional N N N N N ನ Note 2, 3, 4 Musculo-skeletal Superficial N N N N N N Note 2, 3, 4 Intravascular Cardiac Adult Cardiac Pediatric Intravascular (Cardiac) Trans-esoph. (Cardiac) Intra-Cardiac Peripheral Vascular N N N મ N N Note 2, 3, 4 Other (specify)*** Nenew indication; P previously cleared by FDA; E-added under Appendix E Additional comments: Combined modes: B+M, PW+B, Color + B, PW+Color+B, PW +Color+B, Power + PW+B, * Intraoperative includes abdominal, thoracic, and vascular etc. ** Small organ-breast, thyroid, testes, etc. *** Other use includes Urology. Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. Note 2: Smart3D Note 3: iScape Note 4: iBeam Diagnostic Ultrasound Indications for Use Form (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation(ODE) Hela lemm on of Reproductive, Abdominal Radiological Device 510(k) Number {16}------------------------------------------------ Mindray Co. Ltd.- DC-3/DC-3T Diagnostic Ultrasound System Diagnostic Ultrasound Indications for Use Form | System | | |--------|---| | Model: | - | ## 7LT4 Koda Spe Transducer × 510(k) Number(s) | Clinical Application | Mode of Operation | | | | | | | | |--------------------------------------------------------------------------------------------------|-------------------|---|-----|-----|------------------|----------------------|-----------------------|-----------------| | | B | M | PWD | CWD | Color<br>Doppler | Amplitude<br>Doppler | Combined<br>(specify) | Other (specify) | | Ophthalmic | | | | | | | | | | Fetal | | | | | | | | | | Abdominal | N | N | N | | N | N | N | Note 2, 3, 4 | | Intraoperative (specify)* | N | N | N | | N | N | N | Note 2, 3, 4 | | Intraoperative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | | Pediatric | N | N | N | | N | N | N | Note 2, 3, 4 | | Small organ(specify)** | N | N | N | | N | N | N | Note 2, 3, 4 | | Neonatal Cephalic | | | | | | | | | | Adult Cephalic | | | | | | | | | | Trans-rectal | | | | | | | | | | Trans-vaginal…
Innolitics

Panel 1

/
Sort by
Ready

Predicate graph will load when search results are available.

Embedding visualization will load when search results are available.

PDF viewer will load when search results are available.

Loading panels...

Select an item from the tree

Click any panel, subpart, regulation, product code, or device to see details here.

Section Matches

Results will appear here.

Product Code Matches

Results will appear here.

Special Control Matches

Results will appear here.

Loading collections...