510(k) K091841 ยท DQY Catheter, Percutaneous
BRIDGEPOINT MEDICAL CROSSBOSS CATHETER, MODEL M-2000
| Applicant | Bridgepoint Medical, Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 2, 2009 |
| Received | Jun 22, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091841
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.