510(k) K083313 ยท DQY Catheter, Percutaneous
WILDCAT 7F GUIDEWIRE SUPPORT CATHETER
| Applicant | Avinger, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Feb 2, 2009 |
| Received | Nov 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083313
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.