510(k) K112579 ยท DQY Catheter, Percutaneous
WILDCAT 5F GUIDEWIRE SUPPORT CATHETER
| Applicant | Avinger, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Oct 6, 2011 |
| Received | Sep 6, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112579
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.