510(k) K960866 ยท KNY Accessories, Catheter, G-U
LRM PRODUCES GUIDEWIRES ON AN OEM BASIS FOR MANUFACTURERS,KIT ASSEMBLERS, AND DISTRIBUTORS.
| Applicant | Lake Region Mfg., Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Apr 5, 1996 |
| Received | Mar 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960866
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.