510(k) K092298 ยท DQY Catheter, Percutaneous
MODIFICATION TO MODIFIED HD GUIDE CATHETER
| Applicant | Concentric Medical, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Nov 5, 2009 |
| Received | Jul 29, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092298
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.