Medical Device Manufacturer · US , San Luis Obispo , CA

U. S. Diagnostics, Inc. - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 1986

22

Total

22

Cleared

0

Denied

FDA 510(k) Regulatory Record - U. S. Diagnostics, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Oct 03, 1986

ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST

General & Plastic Surgery · 81d