510(k) K936235 ยท FMI Needle, Hypodermic, Single Lumen
NEEDLESAFE II & NEEDLEGARD II
| Applicant | Ingenious Technologies Corp., Massillon OH, US |
| Decision | Substantially Equivalent, Mar 28, 1994 |
| Received | Dec 24, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K936235
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.