Medical Device Manufacturer · US , Washington , DC

Minrad, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1997

14

Total

14

Cleared

0

Denied

FDA 510(k) Regulatory Record - Minrad, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Dec 07, 2001

LIGHT SABER INTRODUCER NEEDLE

General & Plastic Surgery · 88d