Bridge Medical, Inc. is one of 20513 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bridge Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CROSSBOSS CATHETER MODEL M-2000, STINGRAY ORIENTING BALLOON CATHETER MODEL M-1000, STINGRAY GUIDEWIRE MODEL M-3004 AND M, BRIDGE SENTRY BEDSIDE UNIT, BRIDGE SENTRY ADMINISTRATION SET-STANDARD CONFIGURATION, BRIDGE SENTRY ADMINISTRATION SET 5
2
Total
2
Cleared
0
Denied
Bridge Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 2 cleared submissions from 1998 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Bridge Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bridge Medical, Inc.
2 devices