Medical Device Manufacturer · US , Mansfield , MA

The Kendall Company, L.P. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - The Kendall Company, L.P. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jan 31, 2000

KERLIX MD ANTIMICROBIAL GAUZE DRESSING

General & Plastic Surgery · 346d