Medical Device Manufacturer · US , Walker , MI

Kinetix - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1983

Total

Cleared

Denied

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

Historical record: 4 cleared submissions from 1983 to 1984. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Kinetix

4 devices

1-4 of 4