Medical Device Manufacturer · US , Stoughton , WI

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

2 submissions · 1 cleared · Since 2007

2

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dermaport, Inc. Gastroenterology & Urology ✕

2 devices

1-2 of 2

Cleared Jul 20, 2009

DERMAPORT PORTED VASCULAR ACCESS SYSTEM (PVAS)

Gastroenterology & Urology · 34d

Cleared Nov 30, 2007

DERMAPORT PERCUTANEOUS VASCULAR ACCESS SYSTEM (PVAS)

Gastroenterology & Urology · 213d