510(k) K895831 ยท FMF Syringe, Piston
NEEDLEPOINT GUARD
| Applicant | Needlepoint Guard, Inc., Grand Island NE, US |
| Decision | Substantially Equivalent, Dec 1, 1989 |
| Received | Oct 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895831
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.