510(k) K980977 ยท DQX Wire, Guide, Catheter
PIOLAX HYDROPHILIC GUIDEWIRE
| Applicant | Piolax Medical Devices, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Oct 27, 1998 |
| Received | Mar 16, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980977
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.