510(k) K173662 ยท DQY Catheter, Percutaneous
speX Support Catheter
| Applicant | Reflow Medical, Inc., San Clemente CA, US |
| Decision | Substantially Equivalent, Dec 20, 2017 |
| Received | Nov 29, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173662
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.