510(k) K082385 ยท DQY Catheter, Percutaneous
CHAPERON GUIDING CATHETER
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Dec 11, 2008 |
| Received | Aug 19, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082385
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.