Medical Device Manufacturer · US , Mansfield , MA

The Kendall Company - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2001

8

Total

8

Cleared

0

Denied

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

3 devices

1-3 of 3

Cleared Aug 09, 2006

KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311

General Hospital · 30d

Cleared Oct 15, 2001

MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE

General Hospital · 171d

Cleared Jan 11, 2001

FILAC FAS TEMP ELECTRONIC THERMOMETER

General Hospital · 80d