510(k) K913141 ยท FMI Needle, Hypodermic, Single Lumen
MEGA MYELOGRAM KIT
| Applicant | Megadyne Medical Products, Inc., Tampa FL, US |
| Decision | Substantially Equivalent, Oct 17, 1991 |
| Received | Jul 16, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913141
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.