DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 Diagnostic

K173471 · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · IYN · Jan 8, 2018 · Radiology

Device Facts

• Record ID: K173471
• Device Name: DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 Diagnostic
• Applicant: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
• Product Code: IYN · Radiology
• Decision Date: Jan 8, 2018
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.1550
• Device Class: Class 2
• Attributes: Pediatric

Intended Use

Diagnostic Ultrasound imaging or fluid flow analysis of the human body as follows:

Device Story

The DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 is a mobile, software-controlled diagnostic ultrasound system. It uses an array of transducers (linear, convex, phased) to transmit ultrasonic energy into the body and process received echoes. The system generates images in B-mode, M-mode, PW-mode, CW-mode, Color-mode, Color M-mode, Power/Dirpower mode, TDI mode, 3D/4D mode, and Elastography, or combined modes (e.g., B/M-mode). It is used in clinical settings by healthcare professionals to visualize anatomic structures and analyze fluid flow. The output is displayed on-screen for clinical assessment, supporting diagnosis and patient management.

Clinical Evidence

No clinical data. Substantial equivalence is supported by bench testing, including acoustic output measurements, biocompatibility, cleaning/disinfection effectiveness, and thermal, electrical, and mechanical safety testing in accordance with recognized standards (e.g., IEC 60601-1, IEC 60601-2-37, ISO 10993-1).

Technological Characteristics

Mobile diagnostic ultrasound system; utilizes linear, convex, and phased array transducers. Supports B, M, PW, CW, Color, Color M, Power/Dirpower, TDI, 3D/4D, and Elastography modes. Complies with IEC 60601-1, IEC 60601-1-2, IEC 60601-2-37, and NEMA UD 2-2004. Software developed per IEC 62304.

Indications for Use

Indicated for adults, pregnant women, pediatric patients, and neonates. Used for fetal, abdominal, pediatric, small organ (breast, thyroid, testes), neonatal cephalic, adult cephalic, trans-rectal, trans-vaginal, musculo-skeletal (conventional, superficial), cardiac adult, cardiac pediatric, peripheral vessel, urology, and transesophageal (cardiac) exams.

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

• DC-8 (K170277)

Reference Devices

• Resona 7 (K171233)
• DC-70 (K163690)
• M9 (K171034)

Submission Summary (Full Text)

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Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.

Shenzhen Mindray Bio-medical Electronics Co., LTD. % Yang Zhaohui Engineer of Technical Regulation Mindray Building, Keji 12th Road South Hi-tech Industrial Park, Nanshan ShenZhen, GangDong 518057 P.R. CHINA

January 8, 2018

Re: K173471

Trade/Device Name: DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 Diagnostic Ultrasound System Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: II Product Code: IYN, IYO, ITX Dated: November 1, 2017 Received: November 8, 2017

Dear Yang Zhaohui:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and 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) that do not require approval of a premarket approval application (PMA). 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to 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); medical device reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820);

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## Page 2 - Yang Zhaohui

and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (http://www.fda.gov/DICE) for more information or contact DICE by email ([e-mail]) or phone [phone] or 301-796-7100).

Sincerely,

Michael D'Hara For

Robert Ochs. Ph.D. Director Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health

Enclosure

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#### Indications for Use

510(k) Number (if known)

K173471

Device Name

DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 Diagnostic Ultrasound System

Indications for Use (Describe)

The DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 Diagnostic Ultrasound System is applicable for adults, pregnant women, pediatric patients and neonates. It is intended for use in fetal, abdominal, pediatric, small organ (breast, thyroid, testes), neonatal cephalic, adult cephalic, trans-raginal, musculo-skeletal (conventional, superficial), cardiac adult, cardiac pediatric, peripheral vessel, urology and transesophageal (Cardiac) exams.

| Type of Use (Select one or both, as applicable) | |
|------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------|
| <span> <span style="font-size: large;">✔</span> Prescription Use (Part 21 CFR 801 Subpart D) </span> | <span> ☐ Over-The-Counter Use (21 CFR 801 Subpart C) </span> |

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| System: | DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 Diagnostic Ultrasound System | | | | | | | | | | |
|-----------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------|-------------------|-----|-----|------------------|----------------------|-----------------------|-----------------------------------|--------------------|-----------------|
| Transducer: | | | | | | | | | | | |
| Intended Use: | Diagnostic Ultrasound imaging or fluid flow analysis of the human body as follows: | | | | | | | | | | |
| Clinical Application Mode of Operation | | | | | | | | | | | |
| General (Track 1 Only) | Specific (Track 1 & 3) | B | M | PWD | CWD | Color Doppler | Amplitude Doppler | Combined (specify) | Other (specify) | | |
| Ophthalmic | Ophthalmic | | | | | | | | | | |
| Fetal Imaging & Other | Fetal | P | P | P | P | P | P | P | Note 1, 2, 3, 4,6,7 | | |
| | Abdominal | P | P | P | P | P | P | P | Note 1, 2, 3, 4, 6, 7, 10, 11, 12 | | |
| | Intra-operative (Specify*) | P | P | P | | P | P | P | Note 1,2,4 | | |
| | Intra-operative (Neuro) | | | | | | | | | | |
| | Laparoscopic | | | | | | | | | | |
| | Pediatric | P | P | P | P | P | P | P | Note 1, 2, 3,4,6,7 | | |
| | Small Organ (Specify**) | P | P | P | | P | P | P | Note 1,2, 4,7,8 | | |
| | Neonatal Cephalic | P | P | P | P | P | P | P | Note 1,2, 4,6,7 | | |
| | Adult Cephalic | P | P | P | P | P | P | P | Note 1, 2,4, 6,7 | | |
| | Trans-rectal | P | P | P | | P | P | P | Note 1, 2, 3,4,6,7,8 | | |
| | Trans-vaginal | P | P | P | | P | P | P | Note 1, 2, 3,4,6,7,8 | | |
| | Trans-urethral | | | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | | | |
| | Musculo-skeletal (Conventional) | P | P | P | P | P | P | P | Note 1, 2, 4,6,7 | | |
| | Musculo-skeletal (Superficial) | P | P | P | | P | P | P | Note 1,2, 4,7 | | |
| | Intravascular | | | | | | | | | | |
| Cardiac | Cardiac Adult | P | P | P | P | P | P | P | Note 1, 2,4,5,6,7,9 | | |
| | Cardiac Pediatric | P | P | P | P | P | P | P | Note 1, 2,4,5,6,7 | | |
| | Intravascular (Cardiac) | | | | | | | | | | |
| | Trans-esoph. (Cardiac) | P | P | P | P | P | P | P | Note 1, 5,6 | | |
| | Intra-cardiac | | | | | | | | | | |
| Peripheral vessel | Peripheral vessel | P | P | P | | P | P | P | Note 1, 2, 4,6,7 | | |
| | Other (Specify***) | P | P | P | | P | P | P | Note 1, 2, 4,6,7 | | |
| | 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 | | | | | | | | | | |
| | ** Small organ-breast, thyroid, testes. | | | | | | | | | | |
| | ***Other use includes Urology. | | | | | | | | | | |
| System: | DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85 Diagnostic Ultrasound System | | | | | | | | | | |
| Transducer: | C5-1E | | | | | | | | | | |
| Intended Use: | Diagnostic Ultrasound imaging or fluid flow analysis of the human body as follows: | | | | | | | | | | |
| Clinical Application | Mode of Operation | | | | | | | | | | |
| General (Track<br>1 Only) | Specific (Track 1 & 3) | B | M | PWD | CWD | Color<br>Doppler | Amplitude<br>Doppler | Combined<br>(specify) | Other (specify) | | |
| Ophthalmic | Ophthalmic | | | | | | | | | | |
| Fetal Imaging<br>& Other | Fetal | P | P | P | | P | P | P | Note 1, 2, 4,6,7 | | |
| | Abdominal | P | P | P | | P | P | P | Note 1, 2, 4, 6, 7,<br>10, 11, 12 | | |
| | Intra-operative (Specify*) | | | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | | | |
| | Laparoscopic | | | | | | | | | | |
| | Pediatric | P | P | P | | P | P | P | Note 1, 2, 4,6,7 | | |
| | Small Organ (Specify**) | | | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | | | |
| | Adult Cephalic | | | | | | | | | | |
| | Trans-rectal | | | | | | | | | | |
| | Trans-vaginal | | | | | | | | | | |
| | Trans-urethral | | | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | | | |
| | Musculo-skeletal<br>(Conventional) | P | P | P | | P | P | P | Note 1, 2, 4,6,7 | | |
| | Musculo-skeletal<br>(Superficial) | | | | | | | | | | |
| | Intravascular | | | | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | | | |
| | Intra-cardiac | | | | | | | | | | |
| Peripheral<br>vessel | Peripheral vessel | P | P | P | | P | P | P | Note 1, 2, 4,6,7 | | |
| | Other (Specify***) | | | | | | | | | | |
| | N=new indication; P=previously cleared by FDA(K171233); E=added under Appendix E | | | | | | | | | | |
| | Additional comments: Combined modes--B+M PW+B Color+B Power + B PW+Color+B Power + PW +B.<br>*Intraoperative includes abdominal, thoracic, and vascular | | | | | | | | | | |
| | **Small organ-breast, thyroid, testes. | | | | | | | | | | |
| | ***Other use includes Urology.<br>Note 1: Tissue Harmonic Imaging. The feature does not use contrast agents. | | | | | | | | | | |
| | Note 2: Smart3D | | | | | | | | | | |
| | Note 3:4D(Real-time 3D) | | | | | | | | | | |
| | Note 4: iScape | | | | | | | | | | |
| | Note 5: TDI | | | | | | | | | | |
| | Note 6: Color M | | | | | | | | | | |
| | Note 7: Biopsy Guidance | | | | | | | | | | |
| | Note 8: Elastography…