510(k) K192253

Device
SonicEye Dual-Array Ultrasound System
Applicant
Sonivate Medical Inc
510(k) number
K192253
Product code
IYO  
Decision
Substantially Equivalent (SESE)
Decision date
2020-02-25
Date received
2019-08-20
Regulation
892.1560
Classification name
System, Imaging, Pulsed Echo, Ultrasonic
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Steve Hesler
Address
4640 SW Macadam Ave. Suite 200 Portland OR US 97239 97239

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00850012978008SonicEye® Dual-Array Ultrasound SystemSONIVATE MEDICAL, INC.2020-05-18

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Legacy Summary

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FDA Review

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