510(k) K936032 ยท DQX Wire, Guide, Catheter
TORQUE DEVICE
| Applicant | Merit Medical Systems, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 15, 1994 |
| Received | Dec 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K936032
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.