510(k) K990936 ยท FMI Needle, Hypodermic, Single Lumen
THE VAULT
| Applicant | Stik Stoppers, Inc., Springfield OR, US |
| Decision | Substantially Equivalent, May 18, 1999 |
| Received | Mar 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990936
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.