Who is the manufacturer of ULTRASOUND SCANNER FLEX FOCUS?

B-K Medical Aps filed the 510(k) submission for ULTRASOUND SCANNER FLEX FOCUS (K123254).

What is the FDA product code for ULTRASOUND SCANNER FLEX FOCUS?

IYN. It is classified under 21 CFR 892.1550 as a Class 2 device in the Radiology panel.

What is the regulatory pathway for ULTRASOUND SCANNER FLEX FOCUS?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like ULTRASOUND SCANNER FLEX FOCUS?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

ULTRASOUND SCANNER FLEX FOCUS

Q: What are the predicate devices for ULTRASOUND SCANNER FLEX FOCUS?

B-K Medical Ultrasound Scanner Flex Focus 1202 (K081154); B-K Medical Ultrasound Scanner Pro Focus 2202 (K100919).

K123254 · B-K Medical Aps · IYN · Feb 13, 2013 · Radiology

Device Facts

Record ID	K123254
Device Name	ULTRASOUND SCANNER FLEX FOCUS
Applicant	B-K Medical Aps
Product Code	IYN · Radiology
Decision Date	Feb 13, 2013
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 892.1550
Device Class	Class 2

Intended Use

Diagnostic ultrasound imaging or fluid flow analysis of the human body.

Device Story

Ultrasound Scanner Flex Focus 1202 is a diagnostic ultrasound system for imaging and fluid flow analysis. It processes acoustic signals from linear, convex, phased, and mechanical sector transducers to generate B-mode, M-mode, PWD, CFM (Color/Power Doppler), and Tissue Harmonic images. Optional modules include 3-D reconstruction of 2-D images and Vector Flow Imaging (VFI) for visualizing axial and transverse velocity. Used in clinical settings (e.g., OR, clinic) by physicians or trained clinicians for diagnostic exams and biopsy guidance. The system performs geometric measurements and calculations. Output is displayed on-screen for real-time clinical decision-making, aiding in diagnosis and interventional procedures. The device supports non-monitoring ECG input for image synchronization.

Clinical Evidence

Bench testing only. The device underwent thermal, mechanical, and electrical safety testing by a recognized Certified Body. Acoustic output reporting complies with FDA guidance 'Information for Manufacturers Seeking Clearance of Diagnostic Ultrasound Systems and Transducers' (2008). No clinical data was required for this 510(k) clearance.

Technological Characteristics

Diagnostic ultrasound system using pulsed echo and Doppler imaging. Transducers: linear, convex, phased, and mechanical sector arrays. Biocompatible patient contact materials. Acoustic output: Track 3, MI ≤ 1.9, Ispta ≤ 720 mW/cm², TI ≤ 6.0. Connectivity: supports non-monitoring ECG input. Software includes geometric measurement and calculation packages, 3-D reconstruction, and Vector Flow Imaging (VFI).

Indications for Use

Indicated for diagnostic ultrasound imaging and fluid flow analysis in abdominal, cardiac, fetal, intraoperative, neurosurgical, obstetric, transrectal, small organ (breast, testis, penis), transvaginal, and musculoskeletal clinical applications. Includes biopsy needle guidance, geometric measurements, and non-monitoring ECG superimposition.

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

B-K Medical Ultrasound Scanner Flex Focus 1202 (K081154)
B-K Medical Ultrasound Scanner Pro Focus 2202 (K100919)

Related Devices

K132677 — ULTRASOUND SCANNER FLEX FOCUS 1202 · B-K Medical Aps · Jan 7, 2014
K132335 — ULTRASOUND SCANNER FLEX FOCUS 1202 · B-K Medical Aps · Jan 10, 2014
K132685 — ULTRASOUND SCANNER PRO FOCUS 2202 · B-K Medical Aps · Jan 6, 2014
K081154 — ULTRASOUND SCANNER FLEX FOCUS, MODEL 1202 · B-K Medical Aps · May 23, 2008
K132346 — ULTRASOUND SCANNER PRO FOCUS 2202 · B-K Medical Aps · Jan 10, 2014

Submission Summary (Full Text)

{0}------------------------------------------------ #### Attachment 4 #### 510(k) Summary: FEB 1 3 2013 This summary is provided as part of this Premarket Notification in compliance with 21CRF, Section 807.92. Submitters name: B-K Medical Address: Mileparken 34, DK2730 Herlev, Denmark Phone: +45 44528100 Fax: +45 44528199 Contact person: Randi Hauerberg, Regulatory Affairs Manager Date prepared: May 9, 2012 Trade name: Ultrasound Scanner Flex Focus 1202 Common name: Diagnostic Ultrasound System Classification names: (90 IYO, CFR 892.1560) Ultrasonic Pulsed Echo Imaging System Ultrasonic Pulsed Doppler Imaging System (90 IYN, CFR 892.1560) Diagnostic Ultrasonic Transducer (90 ITX, CFR 892.1570) Identification of predicate, legally marketed device: B-K Medical Ultrasound Scanner Flex Focus 1202, K081154 B-K Medical Ultrasound Scanner Pro Focus 2202, K100919 #### Device description: Flex Focus 1202 supports the following scanning modes and combinations thereof: B-mode (incl.Tissue Harmonic Imaging), M-mode, PWD mode, CFM mode, Amplitude (Power) Doppler mode. The system can perform simple geometric measurements, and perform calculations in the areas of Vascular, Urology, Cardiology and OB/GYN applications. The system can guide biopsy- and puncture needles. An optional 3-D module can reconstruct a series of 2-D images into a single 3-D volume and display this on the screen. An optional Vector Flow Imaging (VFI) module: Color Flow Mapping (CFM) imaging mode with the ability to visualize both the axial and the transverse velocity. #### Transducers Transducers are linear arrays, convex arrays, phased arrays and mechanical sector. The patient contact materials are biocompatible. All transducers used together with Flex Focus 1202 are Track 3 transducers. #### Acoustic output The system controlling the Acoustic Output in the modified Flex Focus 1202 is the same as the system in Flex Focus 1200. The system will assure that the acoustic output always will stay below the pre-amendments upper limits i.e. Ispta ≤ 720 mW/cm² and MI ≤ 1.9 (Track 3, non ophthalmic). The Thermal Index values are maximum 6.0, i.e. TI ≤ 6.0 {1}------------------------------------------------ #### Attachment 4 #### Clinical measurement accuracy Clinical measurements and calculations are described and accuracies are provided in the User Information. #### Thermal, mechanical and electrical safety. The scanner Flex Focus 1202 has been tested by a recognized Certified Body. #### Acoustic Output Reporting The Acoustic Output Reporting is made according to the standards required by "Information for Manufacturers Seeking Clearance of Diagnostic Ultrasound Systems and Transducers, FDA, CDRH, September 9, 2008" Intended use: Diagnostic ultrasound imaging or fluid flow analysis of the human body. #### Summary of Technological Characteristics – Predicate Device Compared to Modified Device | | Predicate device K081154, Ultrasound scanner Flex Focus 1202 | Predicate device K100919, Ultrasound scanner Pro Focus 2202 | Modified device (this application), Ultrasound scanner Flex Focus 1202 | |--------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Modes of operation Ref.: [1] Appendix G | B, M, PWD, CFM1) and combinations. Tissue harmonic imaging. | B, M, PWD, CFM1)+2) and combinations Tissue harmonic imaging. | B, M, PWD, CFM1)+2) and combinations Tissue harmonic imaging. | | Intended Use: | Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | | Indications For Use: | Abdominal Cardiac Fetal (incl Obstetrics) Intraoperative Transurethral Neurosurgery Pediatrics Transrectal Small Parts (organs) Transvaginal Peripheral vascular Muskulo-skeletal (conventional and superficial) | Abdominal Cardiac Fetal (incl Obstetrics) Intraoperative Transurethral Neurosurgery Pediatrics Transrectal Small Parts (organs) Transvaginal Peripheral vascular Muskulo-skeletal (conventional and superficial) | Abdominal Cardiac Fetal (incl Obstetrics) Intraoperative Transurethral Neurosurgery Pediatrics Transrectal Small Parts (organs) Transvaginal Peripheral vascular Muskulo-skeletal (conventional and superficial) | | Features | | ECG (not monitoring) | | 1) CFM= Color Flow Mapping=Color Doppler and Amplitude (Power) Doppler. {2}------------------------------------------------ ### Attachment 4 2) Includes Vector Flow Imaging ### Technological characteristics compared to the predicate device The predicate device has the same major technological characteristics as the subject device described above. Minor differences consist: Optional Vector Flow Imaging (VFI) module. {3}------------------------------------------------ #### DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/3/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized eagle emblem with three wavy lines representing the department's mission. #### Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-002 February 13, 2013 B-K MEDICAL APS C/O Randi Hauerberg Regulatory Affairs Manager MILEPARKEN 34 DENMARK DK-2730 Re: K123254 Trade/Device Name: Ultrasound Scanner Flex Focus Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic Pulsed Doppler Imaging System Regulatory Class: Class II Product Code: IYN, IYO, and ITX Dated: January 14, 2013 Received: January 16, 2013 Dear Randi Hauerberg: 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. This determination of substantial equivalence applies to the following transducers intended for use with the Ultrasound Scanner Flex Focus 1202, as described in your premarket notification: > Transducer Model Number 8670 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 895. 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 {4}------------------------------------------------ Page 2 - Randi Hauerberg 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 go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH0ffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR 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. If you have any questions regarding the content of this letter, please contact Robert Ochs at (301) 796-6661. Sincerely yours, # Sean M. Boyd -S for Janine M. Morris Director, Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ ### Indications for Use #### 510(k) Number (if known): K123254 Device Name: Ultrasound Scanner Flex Focus 1202 Indications for Use: Ultrasound scanner and transducers for B, Tissue and Contrast Harmonic Imaging, M, PWD, CWD, Color Doppler, Vector Flow Imaging and combined mode imaging. Signal analysis and display. Guidance of biopsy needles, geometrical measurements and calculation of parameters. Non monitoring ECG for superimposing the ultrasound information. An optional 3-D unit can reconstruct a series of 2-D images into a single 3-D volume and display this on the screen. An optional Vector Flow Imaging (VFI) module: Color Flow Mapping (CFM) imaging mode with the ability to visualize both the axial and the transverse velocity. Clinical applications: Abdominal, Cardiac, Fetal, Intraoperative, Neurosurgery, Obstetrics, Transrectal, Small organs, Transvaginal, Musculoskeletal. #### Details on specific Indication for Use forms Prescription Use > (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of In Vitro Diagnostics and Radiological Health (OIR) # Sean M. Boyd -S (Division Sign Off) Division of Radiological Health Office of In Vitro Diagnostic and Radiological Health K123254 510(k) Page 1 of 3 {6}------------------------------------------------ ### Indications for Use ### DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE FORM System:1202 Transducer: 8670 Intended Use; Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | Clinical Application | | Mode of Operation | | | | | | | |---------------------------|---------------------------------|-------------------|---|-----|---------------------------|------------------|-----------------------|----------------------| | General (Track I Only) | Specific (Tracks I & III) | B | M | PWD | Harmonic imaging 2) | Color Doppler | Combined (Specify) | Amplitude Doppler | | Ophthalmic | Ophthalmic | | | | | | | | | | Fetal | | | | | | | | | | Abdominal 2) | | | | | | | | | | Intra-operative (Specify) | | | | | | | | | | Intra-operative (Neuro) | | | | | | | | | | Laparoscopic | | | | | | | | | Fetal Imaging & Other | Pediatric | E | E | E | E | E | E 1) | E | | | Small Organ (Specify) 3) | E | E | E | E | E | E 1) | E | | | Neonatal Cephalic | | | | | | | | | | Adult Cephalic | | | | | | | | | | Trans-rectal | | | | | | | | | | Trans-vaginal | | | | | | | | | Trans-urethral | | | | | | | | | | Trans-esoph. (non-Card.) | | | | | | | | | | | Musculo-skel. (Conventional) | E | E | E | E | E | E 1) | E | | | Musculo-skel. (Superficial) | E | E | E | E | E | E 1) | E | | | Intra-luminal | | | | | | | | | | Other (Specify) | | | | | | | | | Cardiac | Cardiac Adult | | | | | | | | | | Cardiac Pediatric | | | | | | | | | | Trans-esoph. (Cardiac) | | | | | | | | | | Other (Specify) | | | | | | | | | Peripheral Vessel | Peripheral vessel | E | E | E | E | N4) | E 1) | E | | | Other (Specify) | | | | | | | | N= new indication; P= previously cleared by FDA; E= added under Appendix E *Examples may include: A-mode. Amplitude Doppler, 3-D Imaging, Harmonic Imaging, Tissue Motion Doppler, Color Velocity Imaging (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of In Vitro Diagnostics and Radiological Health (OIR) # Sean M. Boyd -S (Division Sign Off) Division of Radiological Health Office of In Vitro Diagnostic and Radiological Health K123254 510(k) > Page 2 of 3 {7}------------------------------------------------ ## Indications for Use 1) Mode combinations: B+M, B+D, B+C, B+D+C. Additional Comments: (D is PWD, C is Color Flow mapping Doppler including Amplitude (power) Doppler). 2) Includes tissue harmonic imaging. 3) Small part: Breast, testis and penis 4) Vector Flow Imaging (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of In Vitro Diagnostics and Radiological Health (OIR) Sean M. Boyd -S (Division Sign Off) . Division of Radiological Health Office of In Vitro Diagnostic and Radiological Health K123254 510(k)_ Page 3 of 3