510(k) K952518 ยท FMI Needle, Hypodermic, Single Lumen
SAFE CAP NEEDLE RECAPPING/UNCAPPING DEVICE
| Applicant | Medi-Dose, Inc., Feasterville PA, US |
| Decision | Substantially Equivalent, Jul 28, 1995 |
| Received | Apr 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952518
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.