Cardinal Health 207, Inc. is one of 18330 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardinal Health 207, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VELA VENTILATOR, HELIOX LOW FLOW SENTRY BLENDER, PURESOM NASAL MASK-SMALL, PURESOM NASAL MASK-MEDIUM, PURESOM NASAL MASK-LARGE, MODELS 11924-01, 11924-02, 11924-03
5
Total
5
Cleared
0
Denied
Cardinal Health 207, Inc. has 5 FDA 510(k) cleared medical devices. Based in Yorba Linda, US.
Historical record: 5 cleared submissions from 2008 to 2010. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Cardinal Health 207, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardinal Health 207, Inc.
5 devices
Cleared
May 11, 2010
VELA VENTILATOR
Anesthesiology
222d
Cleared
Apr 02, 2010
HELIOX LOW FLOW SENTRY BLENDER
Anesthesiology
232d
Cleared
Mar 10, 2010
PURESOM NASAL MASK-SMALL, PURESOM NASAL MASK-MEDIUM, PURESOM NASAL...
Anesthesiology
159d
Cleared
Oct 09, 2008
THE ADVANTAGE SERIES NON-VENTED (NV) FULL FACE MASK
Anesthesiology
118d
Cleared
Aug 13, 2008
AVEA VENTILATOR
Anesthesiology
44d