Medical Device Manufacturer · US , Vernon Hills , IL

Bd - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 2001

15

Total

15

Cleared

0

Denied

FDA 510(k) cleared devices by Bd General Hospital ✕

7 devices

1-7 of 7

Cleared Feb 07, 2003

BD INTEGRA SYRINGE

General Hospital · 91d

Cleared Jul 19, 2002

BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET

General Hospital · 72d

Cleared Mar 20, 2002

BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757

General Hospital · 29d

Cleared Jan 23, 2002

BD PRE-FILLED HEPARIN LOCK FLUSH IN 0.9% SODIUM CHLORIDE INJECTION, USP SYRINGE

General Hospital · 212d

Cleared Jul 17, 2001

0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE

General Hospital · 21d

Cleared Jun 19, 2001

INTERLINK THREADED LOCK CANNULA

General Hospital · 5d

Cleared Jun 13, 2001

BD SPRING BASED SYRINGE

General Hospital · 63d