Medical Device Manufacturer · US , Englewood , CO

Accufix Research Institute - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000
1
Total
1
Cleared
0
Denied

Accufix Research Institute has 1 FDA 510(k) cleared medical devices. Based in Englewood, US.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Accufix Research Institute

1 devices
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