Arizant Healthcare, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arizant Healthcare, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Arizant Healthcare, Inc. has 6 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 6 cleared submissions from 2004 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arizant Healthcare, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arizant Healthcare, Inc.
6 devices
Cleared
May 30, 2012
3M SPOTON TEMPERATURE MONITORING SYSTEM
General Hospital
110d
Cleared
Oct 06, 2008
RANGER RAPID FLOW BLOOD/FLUID WARMING SYSTEM
General Hospital
61d
Cleared
Jun 26, 2006
RANGER IRRIGATION FLUID WARMING SYSTEM
General Hospital
81d
Cleared
Apr 24, 2006
BAIR PAWS TEMPERATURE MANAGEMENT SYSTEM MODEL 850
Cardiovascular
25d
Cleared
Mar 09, 2006
MODIFICATION TO:BAIR HUGGER TEMPERATURE MANAGEMENT SYSTEMS
Cardiovascular
69d
Cleared
Jun 30, 2004
BAIR HUGGER TEMPERATURE MANAGEMENT SYSTEM
Cardiovascular
8d