510(k) K102022 ยท DQY Catheter, Percutaneous
WILDCAT 6F GUIDEWIRE SUPPORT CATHETER MODEL W400L AND W400S
| Applicant | Avinger, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Aug 6, 2010 |
| Received | Jul 19, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102022
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.