510(k) K913317 ยท FMI Needle, Hypodermic, Single Lumen
MEGA ARTHROGRAM KIT
| Applicant | Mega Medical, Inc., Tampa FL, US |
| Decision | Substantially Equivalent, Oct 31, 1991 |
| Received | Jul 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913317
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.