510(k) K971322 ยท DQX Wire, Guide, Catheter
CORE AND COIL ASSEMBLY GUIDEWIRE
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Jul 22, 1998 |
| Received | Apr 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971322
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.