510(k) K960963 ยท FMI Needle, Hypodermic, Single Lumen
CORD WRAP WITH NEEDLE RESHEATHER
| Applicant | Osborn Medical Corp., Utica MN, US |
| Decision | Substantially Equivalent, May 6, 1996 |
| Received | Mar 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960963
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.