Medical Device Manufacturer · US , Omaha , NE

Raven Biological Laboratories, Inc. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1992

15

Total

15

Cleared

0

Denied

Raven Biological Laboratories, Inc. has 15 FDA 510(k) cleared general hospital devices. Based in Omaha, US.

Historical record: 15 cleared submissions from 1992 to 2009.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

Raven Biological Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Raven Biological Laboratories, Inc.

15 devices

1-15 of 15

Cleared Oct 21, 2009

RAVEN PROTEST - STEAM BIOLOGICAL INDICATOR

General Hospital · 397d

Cleared Mar 15, 2007

PROCHEM EXT CHEMICAL INTEGRATOR

General Hospital · 189d

Cleared Feb 15, 2006

General Hospital · 91d

Cleared Mar 23, 2005

MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS

General Hospital · 15d

Cleared Sep 13, 2004

RAVEN PROTEST - EO

General Hospital · 74d

Cleared Aug 09, 2004

RAVEN PROTEST - STEAM

General Hospital · 76d

Cleared May 25, 2004

MODIFICATION TO:RAVEN BACTERIAL SPORE STRIPS

General Hospital · 246d

Cleared Mar 03, 2004

PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA

General Hospital · 330d

Cleared Jan 30, 2002

RAVEN BACTERIAL SPORE STRIPS

General Hospital · 26d

Cleared Mar 30, 2001

PROSPORE2 SELF-CONTAINED BIOLOGICAL INDICATOR

General Hospital · 458d

Cleared May 22, 1997

General Hospital · 35d

Cleared May 20, 1997

General Hospital · 33d

Cleared Sep 18, 1996

PROSPORE(STEARO FOR STEAM STERILIZER)

General Hospital · 86d

Cleared Aug 16, 1996

General Hospital · 172d

Cleared Apr 02, 1992

General Hospital · 282d