510(k) K080987 ยท DQY Catheter, Percutaneous
BRIDGEPOINT MEDICAL STINGRAY DEVICE AND ACCESSORIES
| Applicant | Bridgepoint Medical, Orinda CA, US |
| Decision | Substantially Equivalent, Feb 6, 2009 |
| Received | Apr 7, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080987
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 24, 2012 | Bridgepoint Medical BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescription Only, Manufacturer BridgePoint Medical Inc. 13355 10th Ave N, Suite 110, Plymouth, MN 55441.
St Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.