Medical Device Manufacturer · US , Miami , FL

Osko, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2015

Recent clearances: Edge Air(1417) Digital Flat Panel X-ray Detector, Edge Air Digital Flat Panel X-ray Detector, Edge Digital Flat Panel X-ray Detector

6
Total
6
Cleared
0
Denied

Osko, Inc. has 6 FDA 510(k) cleared medical devices. Based in Miami, US.

Historical record: 6 cleared submissions from 2015 to 2020. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Osko, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Mtechgroup as regulatory consultant.

FDA 510(k) Regulatory Record - Osko, Inc.

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