510(k) K960718 ยท DQX Wire, Guide, Catheter
LRM
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, May 21, 1996 |
| Received | Feb 21, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960718
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.