Medical Device Manufacturer · US , Alameda , CA

Coombs Medical Device Consulting - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007

Recent clearances: ESTECH PERCUTANEOUS INSERTION DILATOR KIT

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Coombs Medical Device Consulting Cardiovascular ✕

1 devices

1-1 of 1

Cleared Oct 24, 2007

ESTECH PERCUTANEOUS INSERTION DILATOR KIT

Cardiovascular · 219d