510(k) K131710 ยท DQX Wire, Guide, Catheter
MERIT HYDROPHILIC GUIDE WIRE
| Applicant | Merit Medical Systems, Inc., Galway, IE |
| Decision | Substantially Equivalent, Jul 29, 2013 |
| Received | Jun 11, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131710
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.