The Sonic Window is intended for the visualization of vessels and vascular access guidance of needles and catheters (Insertion of Peripheral Intra Venous (PIV) Catheters, as an example). The Sonic Window is not indicated for use by a layperson and shall be used by prescription only.

Intended Use: Diagnostic ultrasound imaging and visualization of vessels for vascular access guidance of needles and catheters as follows: Peripheral vascular

Device Description

The Sonic Window with the addition of software to perform and display ultrasound fluid flow analysis is a fully integrated handheld ultrasound imaging system that displays real-time ultrasound images on a coronal plane at a constant depth from the transducer. The depth is controllable by the operator. The Sonic Window system consists of the Sonic Window handheld device, the Docking Station/Charger and the AC Adapter. The Sonic Window uses an imaging mode, C-Mode, which provides the visualization in the coronal plane of peripheral vessels and assessment of vessels width and depth for needle/catheter placement.

AI/ML Overview

Here's a summary of the acceptance criteria and study information based on the provided document:

1. Table of Acceptance Criteria and Reported Device Performance:

The document does not explicitly state numerical acceptance criteria or detail a specific performance study with measured results for the "Sonic Window" device. It generally states that "predetermined acceptance criteria was met" without specifying what those criteria were or the achieved performance values.

2. Sample Size Used for the Test Set and Data Provenance:

The document does not provide any information regarding the sample size used for the test set or the provenance of the data (e.g., country of origin, retrospective/prospective). The studies mentioned are "Performance, verification and validation testing" without specific details about patient data.

3. Number of Experts Used to Establish Ground Truth for the Test Set and Their Qualifications:

The document does not provide any information about the number of experts used or their qualifications for establishing ground truth.

4. Adjudication Method for the Test Set:

The document does not provide any information about the adjudication method used for the test set.

5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study was done, and its Effect Size:

The document does not indicate that an MRMC comparative effectiveness study was done, nor does it provide any effect size for human readers improving with AI vs. without AI assistance. The device description mentions a "C-Mode" for visualization and assessment but doesn't describe AI assistance for human readers.

6. If a Standalone (Algorithm Only Without Human-in-the-Loop Performance) was done:

The document focuses on the device as an imaging system for "visualization of vessels and vascular access guidance." It does not describe a standalone algorithm performance without human-in-the-loop. The system displays images for an operator to use.

7. The Type of Ground Truth Used:

The document does not specify the type of ground truth used. It mentions design validation testing and performance testing but not the method for establishing ground truth for evaluating the device's accuracy in visualizing vessels or guiding access.

8. The Sample Size for the Training Set:

The document does not provide any information regarding the sample size for a training set. The device is described as an ultrasound imaging system, and the submission is a "Special 510(k) Device Modification" which implies changes to an existing device rather than the development of a de novo AI algorithm with specific training data.

9. How the Ground Truth for the Training Set was Established:

As no training set is described, the document does not provide any information on how ground truth for a training set was established.

Summary

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

June 15, 2016

Analogic Corporation % Mr. Michael Doyle Global Director Regulatory & Clinical Affairs 8 Centennial Drive PEABODY MA 01960

Re: K161342

Trade/Device Name: Sonic Window Regulation Number: 21 CFR 892.1560 Regulation Name: Ultrasonic pulsed echo imaging system Regulatory Class: II Product Code: IYO, ITX, IYN Dated: May 17, 2016 Received: May 18, 2016

Dear Mr. Doyle:

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. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638 2041

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or (301) 796-7100 or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. 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.

You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address

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

Sincerely yours,

Robert Oolo

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)

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Device Name Sonic Window

Indications for Use (Describe)

Form Approved: OMB No. 0910-0120 Expiration Date: January 31, 2017 See PRA Statement below.

Type of Use (Select one or both, as applicable)
-------------------------------------------------

Prescription Use (Part 21 CFR 801 Subpart D)

Over-The-Counter Use (21 CFR 801 Subpart C)

CONTINUE ON A SEPARATE PAGE IF NEEDED.

This section applies only to requirements of the Paperwork Reduction Act of 1995.

DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.

The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:

Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov

"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."

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Ultrasound Indications for Use Table

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

System: Sonic Window (SW1000)

Intended Use: Diagnostic ultrasound imaging and visualization of vessels for vascular access guidance of needles and catheters as follows:

	Mode of Operation
Clinical Application	B	M	PWD	CWD	Color Doppler	Combined (Specify)	Other* (Specify)
Peripheral vascular							N*

*= Coronal plane (Constant Imaging Depth Plane)

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

Concurrence of CDRH; Office of In Vitro Diagnostics and Radiological Health (OlR)

Prescription Use (Per 21 CFR 801.109)

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Image /page/4/Picture/0 description: The image contains the logo for Analogic. The word "analogic" is written in a blue sans-serif font. Below the word "analogic" is the phrase "Innovative Solutions for Life" in a smaller font. To the right of the word "analogic" is a blue sphere with a white sine wave running through it.

510(k) Summary 8.

This 510(k) Summary is being submitted in accordance with the requirements of the Safe Medical Device Act (SMDA) of 1990. The content contained in this 510(k) summary has been provided in conformance with 21 CFR 807.92

A. Submitter's information

Name:	Analogic Corporation
Address:	8 Centennial DrivePeabody, MA 01960United States
FDA Establishment Owner /Operator Number:	1220672
Contact person:	Michael J. Doyle
Phone:	978-326-4410
Fax:	978-977-6809
Manufacturer:	Analogic Corporation8 Centennial DrivePeabody, MA 01960United States
Device Name:
Trade/Proprietary Name:	Sonic Window
Common Name:	Ultrasound system
Classification name:	Ultrasonic Pulsed Echo Imaging System
Regulation Medical Specialty:	Radiology
Review Panel:	Radiology
Product Code:	IYO, ITX, IYN
Regulation Number:	892.1560, 892.1570, and 892.1550
Device Classification:	2
Submission type:	Special 510(k)

SW1000

C. Substantial Equivalence:

Model:

This submission is a Special 510(k) Device Modification as described in the FDA's Guidance document entitled, "The New 510(k) Paradigm - Alternate Approaches to Demonstrating Substantial Equivalence in Premarket Notifications". In support of this Special 510(k), Analogic Corporation has provided certification of compliance to 21 CFR §820.30 Design Control requirements. Design validation testing was performed to ensure that the Sonic Window with modifications meets design specifications. The Sonic Window with modifications has been compared to the legally marketed predicate device as cleared through K140126 (March 4, 2014) and was found to be substantially equivalent.

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Image /page/5/Picture/0 description: The image contains the logo for Analogic. The logo features the word "analogic" in a blue, sans-serif font. Above and to the right of the word is a blue sphere with a white sine wave running through it. Below the word "analogic" is the tagline "Innovative Solutions for Life" in a smaller, red font.

D. Device Description/Indications for Use:

Indications for Use:

E. Technological Characteristics

The proposed device has the same technological characteristics and is similar in design and configuration as compared to the currently marketed predicate device.

F. Summary of Non-clinical Test/Performance Testing - Bench:

Analogic Corporation believes that the information and data provided in this submission clearly describes the proposed device and demonstrates that the device is adequately designed for the labeled indication for use. Performance, verification and validation testing was conducted to characterize performance of the proposed device and the predetermined acceptance criteria was met. Results of this testing have confirmed that the proposed device is substantially equivalent to the predicate device and is suitable for the labeled indication for use.

Acoustic output:

The Sonic Window transducer system controlling the acoustic output is equivalent to the predicate device. The system will assure that the acoustic output will always stay below the pre-amendment upper limits i.e. Ispta < 720 mW/cm- and MI < 1.9.

The Acoustic Output reporting is made according to the standards required by the FDA Guidance: "Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound Systems and Transducers (September 9, 2008)".

Regulation Number and Section

§ 892.1560 Ultrasonic pulsed echo imaging system.

(a)
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.(b)
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.