Medical Device Manufacturer · US , Mission Viejo , CA

Vertelink Corporation - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2003

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Vertelink Corporation Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Sep 03, 2003

PATHWAY ACCESS SHEATH CATHETER

Gastroenterology & Urology · 184d