510(k) K101647 ยท DQY Catheter, Percutaneous
WILDCAT 5F GUIDEWIRE SUPPORT CATHETER, MODE W500
| Applicant | Avinger, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Aug 6, 2010 |
| Received | Jun 11, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101647
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.