Medical Device Manufacturer · US , Minneapolis , MN

Ascentec Medical Systems - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1991
1
Total
1
Cleared
0
Denied

Ascentec Medical Systems has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 1 cleared submissions from 1991 to 1991. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Ascentec Medical Systems

1 devices
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