Medical Device Manufacturer · US , Mansfield , MA

Covidien Lp, Formerly Registered AS Kendall - FDA 510(k) Cleared Devi...

3 submissions · 2 cleared · Since 2009

3

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Covidien Lp, Formerly Registered AS Kendall General Hospital ✕

1 devices

1-1 of 1

Cleared Apr 17, 2013

MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.

General Hospital · 30d