510(k) K955748 ยท FMI Needle, Hypodermic, Single Lumen
DOYLE EXTRACTOR
| Applicant | Safetech Intl., Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Mar 14, 1996 |
| Received | Dec 15, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955748
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.