510(k) K083343 ยท DQY Catheter, Percutaneous
HEADWAY 17 MICROCATHETER
| Applicant | MicroVention, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Dec 4, 2008 |
| Received | Nov 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083343
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.