ULTRASOUND SCANNER PRO FOCUS 2202

K132346 · B-K Medical Aps · IYO · Jan 10, 2014 · Radiology

Device Facts

• Record ID: K132346
• Device Name: ULTRASOUND SCANNER PRO FOCUS 2202
• Applicant: B-K Medical Aps
• Product Code: IYO · Radiology
• Decision Date: Jan 10, 2014
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 892.1560
• Device Class: Class 2
• Attributes: Pediatric

Intended Use

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

Device Story

Ultrasound Scanner Pro Focus 2202 is a diagnostic ultrasound system for imaging and fluid flow analysis. Inputs include ultrasound transducer signals (linear, convex, phased, mechanical sector arrays) and optional ECG signals. The system processes these signals to perform B-mode (including Tissue Harmonic Imaging), M-mode, PWD, CWD, Color Doppler, and Amplitude (Power) Doppler. Optional modules include 3D reconstruction of 2D images and Vector Flow Imaging (VFI) for axial and transverse velocity visualization. The device supports biopsy and puncture needle guidance, geometric measurements, and parameter calculations. Used in clinical settings by healthcare professionals. Output is displayed on-screen; optional RF wireless function enables transmission for printing and archiving. The device aids clinicians in diagnostic decision-making across various anatomical applications.

Clinical Evidence

Bench testing only. The device was evaluated for acoustic output, thermal, electrical, electromagnetic, and mechanical safety per standards including AIUM/NEMA UD-2, UD-3, IEC 60601-1, IEC 60601-2-37, and IEC 62359. RF wireless function performance was validated through testing at five clinical sites to ensure no interference with system operation. No clinical data was required or provided.

Technological Characteristics

Diagnostic ultrasound system using linear, convex, phased, and mechanical sector arrays. Biocompatible patient contact materials. Acoustic output limited to Ispta ≤ 720 mW/cm² and MI ≤ 1.9 (Track 3). Thermal Index TI ≤ 6.0. Connectivity includes optional RF wireless for printing/archiving. Complies with IEC 60601-1, IEC 60601-1-2, IEC 60601-2-37, and ISO 14971. Software lifecycle processes follow IEC 62304.

Indications for Use

Indicated for diagnostic ultrasound imaging and fluid flow analysis in patients requiring examination of the following clinical applications: Abdominal, Cardiac, Fetal (Obstetrics), Intraoperative, Neurosurgery, Pediatrics, Transrectal, Small organs, Transvaginal, Transurethral, Peripheral vascular, and Musculoskeletal (conventional and superficial).

Regulatory Classification

Identification

An ultrasonic pulsed echo imaging system is a device intended to project a pulsed sound beam into body tissue to determine the depth or location of the tissue interfaces and to measure the duration of an acoustic pulse from the transmitter to the tissue interface and back to the receiver. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

Special Controls

*Classification.* Class II (special controls). A biopsy needle guide kit intended for use with an ultrasonic pulsed echo imaging system only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.

Predicate Devices

• B-K Medical Ultrasound Scanner Pro Focus 2202 (K043524)
• B-K Medical Ultrasound Scanner Pro Focus 2202 (K100919)

Reference Devices

• Adult Cephalic (K070077)

Submission Summary (Full Text)

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K132346
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# 510(k) Summary:

This summary is provided as part of this Premarket Notification in compliance with 21 CRF, Section 807.92.

Submitters name: B-K Medical Address: Mileparken 34, DK2730 Herlev, Denmark Phone: [phone] Fax: [phone] Contact person: Randi Hauerberg, Regulatory Affairs Lead Manager Date prepared: July 19, 2013

Trade name: Ultrasound Scanner Pro Focus 2202 Common name: Diagnostic Ultrasound System Classification names: Ultrasonic Pulsed Echo Imaging System (90 IYO, CFR 892.1560) Ultrasonic Pulsed Doppler Imaging System (90 IYN. CFR 892.1560) Diagnostic Ultrasonic Transducer (90 ITX, CFR 892.1570)

ldentification of predicate, legally marketed device: B-K Medical Ultrasound Scanner Pro Focus 2202, K043524 B-K Medical Ultrasound Scanner Pro Focus 2202, K100919

#### Device description:

Pro Focus 2202 supports the following scanning modes and combinations thereof: B-mode (incl.Tissue Harmonic Imaging), M-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.

An optional ECG signal can be superimposed the ultrasound information in all modes and mode combinations.

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.

An optional RF wireless function with the ability to wireless transmit for printing and archive purpose.

JAN 10 2014

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# Transducers

Transducers are linear arrays, convex arrays, phased arrays and mechanical sector. The patient contact materials are biocompatible.

All transducers used together with Pro Focus 2202 are Track 3 transducers.

#### Acoustic output

The system controlling the Acoustic Output in the modified Pro Focus 2202 is the same as the system in Pro Focus 2202. 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

#### Clinical measurement accuracy

Clinical measurements and calculations are described and accuracies are provided in the User Information.

## Thermal, mechanical and electrical safety.

The scanner Pro Focus 2202 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.

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Summary of Technological Characteristics - Predicate Device Compared to Modified Device

| | Predicate device | Predicate device | Modified device (this application) |
|--------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | K0043524,<br>Ultrasound scanner<br>Pro Focus 2202 | K100919,<br>Ultrasound scanner<br>Pro Focus 2202 | Ultrasound scanner<br>Pro Focus 2202 |
| Modes of operation<br>Ref.: [1] Appendix G | B. M. PWD, CFM 11<br>and combinations<br>Tissue harmonic<br>imaging. | B. M. PWD, CFM 1)+2) and combinations<br>Tissue harmonic<br>imaging. | B. M. PWD. CFM 1)+2)+3) and<br>combinations<br>Tissue harmonic<br>imaging. |
| Intended Use: | Diagnostic ultrasound<br>imaging or fluid flow<br>analysis of the human<br>body as follows: | Diagnostic ultrasound<br>imaging or fluid flow<br>analysis of the human<br>body as follows: | Diagnostic ultrasound<br>imaging or fluid flow<br>analysis of the human<br>body as follows: |
| Indications For Use: | Abdominal<br>Cardiac<br>Fetal (incl Obstetrics)<br>Intraoperative<br>Transurethral<br>Neurosurgery<br>Pediatrics<br>Transrectal<br>Small Parts (organs)<br>Transvaginal<br>Peripheral vascular<br>Muskulo-skeletal<br>(conventional and<br>superficial) | Abdominal<br>Cardiac<br>Fetal (incl Obstetrics)<br>Intraoperative<br>Transurethral<br>Neurosurgery<br>Pediatrics<br>Transrectal<br>Small Parts (organs)<br>Transvaginal<br>Peripheral vascular<br>Muskulo-skeletal<br>(conventional and<br>superficial) | Abdominal<br>Cardiac<br>Fetal (incl Obstetrics)<br>Intraoperative<br>Transurethral<br>Neurosurgery<br>Pediatrics<br>Transrectal<br>Small Parts (organs)<br>Transvaginal<br>Peripheral vascular<br>Muskulo-skeletal<br>(conventional and<br>superficial) |
| Features | ECG (not monitoring) | ECG (not monitoring) | ECG ((not monitoring) |

1) CFM= Color Flow Mapping=Color Doppler and Amplitude (Power) Doppler.

- 2) Includes Vector Flow Imaging
- 3) Includes RF wireless function

# A brief discussion of non-clinical tests submitted, referenced, or relied on in the 510(k) for a determination of substantial equivalence.

The device has been evaluated for acoustic output, thermal, electrical, electromagnetic and mechanical safety and has been found to conform with applicable medical device safety standards. The system complies with the following voluntary standards:

- AIUM/NEMA UD-2, Acoustic Output Measurement Standard For Diagnostic Ultrasound . Equipment
- AIUM/NEMA UD-3, Real-time Display of Thermal and Mechanical Acoustic Output . Indices on Diagnostic Ultrasound Equipment
- IEC 60601-1, Medical Electrical Equipment, Part 1: General requirements for safety .
- IEC 60601-1-1. General requirements for safety, Part 1:1, Collateral Standard. Safety . requirements for medical electrical systems,

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K132346
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- . IEC 60601-1-2. General requirements for safety, Collateral Standard. Electromagnetic Compatibility - Requirements and tests
- IEC 60601-2-37, Particular requirements for the safety of ultrasonic diagnostic medical and monitoring equipment
- ISO 14971, Application of Risk Management of Medical Devices .
- IEC 62304, Medical Device Software Software lifecycle processes .
- IEC 62359, Ultrasonics Field characterization Test methods for the determination of . thermal and mechanical indices related to medical diagnostic ultrasonic fields -

Cleared patient contact materials, electrical and mechanical safety are unchanged.

Additional testing of the RF wireless function was performed at five (5) different sites representing actual user requirements. Several test scenarios was performed and no interference was measured.

## 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 RF wireless function.

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DEPARTMENT OF HEALTH & HUMAN SERVICES

Image /page/4/Picture/1 description: The image contains a circular seal or logo. The seal features the emblem of the U.S. Department of Health & Human Services (HHS). The HHS emblem is a stylized depiction of an eagle or bird-like figure with three curved lines representing its wings or feathers. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged around the upper perimeter of the circle.

Public Health Service

Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

January 10, 2014

B-K Medical ApS % Mrs. Randi Hauerberg Regulatory Affairs Lead Manager Mileparken 34 Herlev DK-2730 DENMARK

Re: K132346

Trade/Device Name: Ultrasound Scanner Pro Focus 2202 Regulation Number: 21 CFR 892.1560 Regulation Name: Ultrasonic pulsed echo imaging system Regulatory Class: II Product Code: IYO, IYN, ITX Dated: November 22, 2013 Received: December 9, 2013

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

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# Page 2-Mrs. Hauerberg

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Small Manufacturers, International and Consumer Assistance at its tollfree number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/Resources/or You/Industry/default.htm. 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/McdicalDevices/Safety/ReportaProblem/dcfault.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

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 [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industrv/default.htm.

Sincerely yours,

for .

Janine M. Morris 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): K132346

#### Device Name: Ultrasound Scanner Pro Focus 2202

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.

An optional RF wireless function with the ability to wireless transmit for printing and archive connectivity purpose.

Clinical applications: Abdominal, Cardiac, Fetal, Intraoperative, Neurosurgery, Obstetrics, Pediatrics, Transrectal, Small organs, Transvaginal, Musculoskeletal.

#### Details on specific Indication for Use forms

Prescription Use X AND/OR Over-The-Counter Use (Part 21 CFR 801 Subpart D) (21 CFR 801 Subpart C)

# (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE) Page 1 of 2

> (Division Sign-Off) Division of Radiological Health/OIR 510(k) _______________________________________________________________________________________________________________________________________________________________________

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#### Diagnostic Ultrasound Indications for Use Form

## System: 2202

: • • •

# Fill out one form for each ultrasound system and each transducer.

Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

| Clinical Application | Mode of Operation | | | | | | | | | |
|----------------------------------------------------------------------------|-------------------|---|---|-----|--------------------------------|------------------|----------------------|------------------------------|-------------------------|---------|
| | A | B | M | PWD | Tissue-<br>harmonic<br>imaging | Color<br>Doppler | Amplitude<br>Doppler | Color<br>Velocity<br>Imaging | Combined<br>(specify 1) | Other4) |
| Ophthalmic | | | | | | | | | | |
| Fetal 2) (K043524) | P | P | P | P | P | P | P | | P | |
| Abdominal (K043524) | P | P | P | P | P | P | P | | P | |
| Intraoperative<br>(K043524) (specify) | P | P | P | P | P | P | P | | P | |
| Intraoperative Neurological<br>(K043524) | P | P | P | P | P | P | P | | P | |
| Pediatric (K043524) | P | P | P | P | P | P | P | | P | |
| Small Organ (K043524) (specify) | P | P | P | P | P | P | P | | P | |
| Neonatal Cephalic | | | | | | | | | | |
| Adult Cephalic (K070077) | P | P | P | P | P | P | P | | P | |
| Cardiac (K043524) | P | P | P | P | P | P | P | | P | |
| Transesophageal | | | | | | | | | | |
| Transrectal (K043524) | P | P | P | P | P | P | P | | P | |
| Transvaginal (K043524) | P | P | P | P | P | P | P | | P | |
| Transurethral (K043524) | P | P | P | P | P | P | P | | P | |
| Intravascular | | | | | | | | | | |
| Peripheral Vascular<br>(K043524) (K100919) | P | P | P | P | P | P1 | P | | P | |
| Laparoscopic | | | | | | | | | | |
| Musculo-skeletal<br>Conventional (K043524) | P | P | P | P | P | P | P | | P | |
| Musculo-skeletal Superficial<br>(K043524) | P | P | P | P | P | P | P | | P | |
| Other (specify) | | | | | | | | | | |
| RF Wireless | | | | | | | | | | N4 |
| N= new indication; P= previously cleared by FDA; E= added under Appendix E | | | | | | | | | | |

Additional Comments:__________________________________________________________________________________________________________________________________________________________

B+M, B+D. B+C, B+D+C. B mode includes Tissue Harmonic Imaging

D is PWD, C is Color Doppler.

Fetal is often called Obstetrics 2)

Vector Flow Imaging ਤੇ

4) RF wireless function

#### (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTKER PAGE IF NEEDED) Concurrence of CDRH .

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