Medical Device Manufacturer · US , Walker , MI

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

5 submissions · 4 cleared · Since 1985
5
Total
4
Cleared
0
Denied

Viratek, Inc. has 4 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 4 cleared submissions from 1985 to 1990. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Viratek, Inc.
5 devices
1-5 of 5
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