510(k) K905305 ยท FMI Needle, Hypodermic, Single Lumen
SAFE-SITE NEEDLE COVER
| Applicant | North American Medical Products, Inc., Loudonville NY, US |
| Decision | Substantially Equivalent, Feb 12, 1991 |
| Received | Nov 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905305
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.