510(k) K172236 ยท MCW Catheter, Peripheral, Atherectomy
Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled
| Applicant | Avinger, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Oct 30, 2017 |
| Received | Jul 25, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172236
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.