Medical Device Manufacturer · US , Oklahoma City , OK

Urocor, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999

Recent clearances: `BI I-125 BRACHYTHERAPHY SEED, MODEL 125SL & 125SH

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Urocor, Inc. Radiology ✕

1 devices

1-1 of 1

Cleared Apr 16, 1999

`BI I-125 BRACHYTHERAPHY SEED, MODEL 125SL & 125SH

Radiology · 123d