Circulatory Technology, Inc. is one of 5124 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Circulatory Technology, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Circulatory Technology, Inc. has 9 FDA 510(k) cleared medical devices. Based in Oyster Bay, US.
Historical record: 9 cleared submissions from 1994 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Circulatory Technology, Inc. Filter by specialty or product code using the sidebar.
Circulatory Technology, Inc. — FDA 510(k) Products and Clearance History
9 devices
Cleared
Apr 17, 2014
INITARY BETTER BLADDER-PEDIATRIC
Cardiovascular
58d
Cleared
Nov 05, 2001
THE V BAG, CATALOG NUMBER VB1800
Cardiovascular
66d
Cleared
Jul 07, 2000
THE V-BAG
Cardiovascular
21d
Cleared
Aug 12, 1998
BETTER-BLADDER (BB)
Cardiovascular
126d
Cleared
Apr 08, 1998
BETTER-TUBING
Cardiovascular
537d
Cleared
May 23, 1997
BETTER-BLADDER (BB)
Gastroenterology & Urology
204d
Cleared
Sep 05, 1996
BETTER-VENTER
Cardiovascular
134d
Cleared
Oct 26, 1994
PRESSURE RELIEF VALVE
Cardiovascular
212d
Cleared
Aug 25, 1994
PRESSURE INFUSION CUFF
General Hospital
64d