510(k) K090335 ยท DQY Catheter, Percutaneous
HD GUIDE CATHETER
| Applicant | Concentric Medical, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, May 6, 2009 |
| Received | Feb 10, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090335
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.