510(k) K090679 ยท MVR Device, Anastomotic, Microvascular
VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM
| Applicant | Vioptix, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Apr 17, 2009 |
| Received | Mar 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090679
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.