510(k) K920717 ยท FMI Needle, Hypodermic, Single Lumen
NEEDLEGARD II
| Applicant | Ingenious Technologies Corp., Massillon OH, US |
| Decision | Substantially Equivalent, Apr 22, 1992 |
| Received | Feb 18, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920717
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.