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 Hospital ✕

3 devices

1-3 of 3

Cleared Aug 26, 2004

SABRESOURCE DRAPE

General Hospital · 49d

Cleared Aug 07, 1998

LIGHT SABER ASPIRATION NEEDLE

General Hospital · 60d

Cleared Jun 25, 1998

MINRAD DRTS LIGHT SABER SYRINGE

General Hospital · 87d