510(k) K170933 ยท DQX Wire, Guide, Catheter
Merit Hydrophilic Guide Wire
| Applicant | Merit Medical Systems, Inc., Galway, IE |
| Decision | Substantially Equivalent, Jun 22, 2017 |
| Received | Mar 29, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K170933
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.