Medical Device Manufacturer · US , Durham , NC

Weck - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Weck General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Feb 26, 2003

HEM-O-LOK XL CLIP

General & Plastic Surgery · 27d

Cleared Aug 14, 2002

WECK HEM-O-LOK AUTOMATIC LIGATING CLIP APPLIER

General & Plastic Surgery · 72d