510(k) K132542 ยท DQY Catheter, Percutaneous
TRANSGATE GUIDE CATHETER
| Applicant | Stryker Neurovascular, Fremont CA, US |
| Decision | Substantially Equivalent, Nov 15, 2013 |
| Received | Aug 13, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132542
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.