Medical Device Manufacturer · US , Mansfield , MA

Kendall - FDA 510(k) Cleared Devices

12 submissions · 10 cleared · Since 2004

12

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kendall General Hospital ✕

1 devices

1-1 of 1

Cleared Dec 10, 2004

KENDALL ARGYLE 2 FR DOUBLE LUMEN NEONATAL/PEDIATRIC PICC, MODEL 43304

General Hospital · 91d