Medical Device Manufacturer · US , Pomfret Center , CT

Universal Fiberoptic Repair, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998
1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Universal Fiberoptic Repair, Inc. General & Plastic Surgery

1 devices
1-1 of 1
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