Bridgepoint Medical is one of 19585 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bridgepoint Medical - FDA 510(k) Cleared Devices
Recent clearances: STINGRAY GUIDEWIRES, MANTARAY GUIDEWIRES, BIGBOSS CATHETERS MANTATAY CATHETER MANTARAY GUIDEWIRES
14
Total
14
Cleared
0
Denied
Bridgepoint Medical has 14 FDA 510(k) cleared cardiovascular devices. Based in Orinda, US.
Historical record: 14 cleared submissions from 2008 to 2012.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Bridgepoint Medical
14 devices
Cleared
Nov 08, 2012
STINGRAY GUIDEWIRES
Cardiovascular
57d
Cleared
Jul 13, 2012
MANTARAY GUIDEWIRES
Cardiovascular
29d
Cleared
CT
May 22, 2012
BIGBOSS CATHETERS MANTATAY CATHETER MANTARAY GUIDEWIRES
Cardiovascular
90d
Cleared
Apr 18, 2012
MANTARAY GUIDEWIRES
Cardiovascular
26d
Cleared
Feb 03, 2012
MANTARAY CATHETER
Cardiovascular
17d
Cleared
Jan 04, 2012
BIGBOSS CATHETER
Cardiovascular
30d
Cleared
Aug 10, 2011
BRIDGEPOINT MEDICAL MANTARAY(TM) CATHETER
Cardiovascular
30d
Cleared
Jun 30, 2011
MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003
Cardiovascular
30d
Cleared
Aug 06, 2010
STINGRAY ORIENTING BALLOON CATHETER
Cardiovascular
60d
Cleared
Sep 02, 2009
BRIDGEPOINT MEDICAL CROSSBOSS CATHETER, MODEL M-2000
Cardiovascular
72d
Cleared
May 14, 2009
BRIDGEPOINT MEDICAL CROSSBOSS PERCUTANEOUS CORONARY CATHETER
Cardiovascular
388d
Cleared
Feb 20, 2009
STINGRAY GUIDEWIRE, STIFF, MODELS M-3003, M-3004, M-3011, M-3012
Cardiovascular
67d