Medical Device Manufacturer · US , Minneapolis , MN

Neomedic International - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2011

Recent clearances: SURELIFT PROLAPSE SYSTEM

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Neomedic International Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Jul 07, 2011

SURELIFT PROLAPSE SYSTEM

Obstetrics & Gynecology · 282d