510(k) K142051 ยท DQX Wire, Guide, Catheter
PRELUDE PLASTIC JACKETED GUIDE WIRE
| Applicant | Merit Medical Systems, Inc., Galway, IE |
| Decision | Substantially Equivalent, Dec 17, 2014 |
| Received | Jul 28, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142051
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.