510(k) K933601 ยท FMI Needle, Hypodermic, Single Lumen
FLIPTIP SAFETY NEEDLE
| Applicant | Syntuition, Inc., Etna NH, US |
| Decision | Substantially Equivalent, Jun 24, 1994 |
| Received | Jul 27, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933601
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.