510(k) K162418 ยท PDU Catheter For Crossing Total Occlusions
Pioneer Plus Catheter
| Applicant | Philips Volcano, San Diego CA, US |
| Decision | Substantially Equivalent, Dec 2, 2016 |
| Received | Aug 30, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K162418
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.