510(k) K072552 ยท DQX Wire, Guide, Catheter
MERIT MEDICAL SYSTEMS, INC., GUIDE WIRE TORQUE DEVICE
| Applicant | Merit Medical Systems, Inc., South Jordan UT, US |
| Decision | Substantially Equivalent, Dec 14, 2007 |
| Received | Sep 10, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072552
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.