FDA 510(k) Applications Submitted by BRIDGEPOINT MEDICAL

FDA 510(k) Number Submission Date Device Name Applicant
K120129 01/17/2012 MANTARAY CATHETER BRIDGEPOINT MEDICAL
K120533 02/22/2012 BIGBOSS CATHETERS MANTATAY CATHETER MANTARAY GUIDEWIRES BRIDGEPOINT MEDICAL
K120881 03/23/2012 MANTARAY GUIDEWIRES BRIDGEPOINT MEDICAL
K111488 05/31/2011 MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003 BRIDGEPOINT MEDICAL
K101591 06/07/2010 STINGRAY ORIENTING BALLOON CATHETER BRIDGEPOINT MEDICAL
K121745 06/14/2012 MANTARAY GUIDEWIRES BRIDGEPOINT MEDICAL
K091841 06/22/2009 BRIDGEPOINT MEDICAL CROSSBOSS CATHETER, MODEL M-2000 BRIDGEPOINT MEDICAL
K111963 07/11/2011 BRIDGEPOINT MEDICAL MANTARAY(TM) CATHETER BRIDGEPOINT MEDICAL
K122795 09/12/2012 STINGRAY GUIDEWIRES BRIDGEPOINT MEDICAL
K113589 12/05/2011 BIGBOSS CATHETER BRIDGEPOINT MEDICAL
K083727 12/15/2008 STINGRAY GUIDEWIRE, STIFF, MODELS M-3003, M-3004, M-3011, M-3012 BRIDGEPOINT MEDICAL
K080987 04/07/2008 BRIDGEPOINT MEDICAL STINGRAY DEVICE AND ACCESSORIES BRIDGEPOINT MEDICAL
K081130 04/21/2008 BRIDGEPOINT MEDICAL CROSSBOSS PERCUTANEOUS CORONARY CATHETER BRIDGEPOINT MEDICAL
K081187 04/28/2008 BRIDGEPOINT MEDICAL ENTERA PERCUTANEOUS CORONARY AND PERIPHERAL GUIDEWIRE, MODEL M-3001 BRIDGEPOINT MEDICAL


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