510(k) K972536 ยท FMI Needle, Hypodermic, Single Lumen
SYRINGE NEEDLE REMOVER (S.N.R.)
| Applicant | Post Medical, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Aug 15, 1997 |
| Received | Jun 8, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972536
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.