Bridgepoint Medical
Bridgepoint Medical holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2012, with 1 FDA device recall on record.
Top product codes for Bridgepoint Medical
FDA recalls by Bridgepoint Medical
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Bridgepoint Medical
- K122795 — STINGRAY GUIDEWIRES
- K121745 — MANTARAY GUIDEWIRES
- K120533 — BIGBOSS CATHETERS MANTATAY CATHETER MANTARAY GUIDEWIRES
- K120881 — MANTARAY GUIDEWIRES
- K120129 — MANTARAY CATHETER
- K113589 — BIGBOSS CATHETER
- K111963 — BRIDGEPOINT MEDICAL MANTARAY(TM) CATHETER
- K111488 — MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003
- K101591 — STINGRAY ORIENTING BALLOON CATHETER
- K091841 — BRIDGEPOINT MEDICAL CROSSBOSS CATHETER, MODEL M-2000
- K081130 — BRIDGEPOINT MEDICAL CROSSBOSS PERCUTANEOUS CORONARY CATHETER
- K083727 — STINGRAY GUIDEWIRE, STIFF, MODELS M-3003, M-3004, M-3011, M-3012
- K080987 — BRIDGEPOINT MEDICAL STINGRAY DEVICE AND ACCESSORIES
- K081187 — BRIDGEPOINT MEDICAL ENTERA PERCUTANEOUS CORONARY AND PERIPHERAL GUIDEWIRE, MODEL M-3001
Data sourced from openFDA. This site is unofficial and independent of the FDA.