510(k) K093160 ยท DQY Catheter, Percutaneous
HEADWAY 21 MICROCATHETER, MODEL: MC212150S
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Nov 5, 2009 |
| Received | Oct 6, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093160
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.