510(k) K990371 ยท FMI Needle, Hypodermic, Single Lumen
DIABETIC NEEDLE DISPOSAL, MODEL # PMSM - 950
| Applicant | Post Medical, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Apr 21, 1999 |
| Received | Feb 8, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990371
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.