Medical Device Manufacturer · US , Indianapolis , IN

Medical Products Div. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006

Recent clearances: HIERSPEC SPECULUM

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medical Products Div. Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Sep 19, 2006

HIERSPEC SPECULUM

Obstetrics & Gynecology · 127d