510(k) K962040 ยท FMI Needle, Hypodermic, Single Lumen
RNS ARTHROGRAM TRAY
| Applicant | Contour Fabricators of Florida, Inc., Tarpon Springs FL, US |
| Decision | Substantially Equivalent, Jun 25, 1996 |
| Received | May 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962040
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.