510(k) K925056 ยท FMI Needle, Hypodermic, Single Lumen
SAFESHARPE (TM) DISPOSAL SYSTEM
| Applicant | Life Medical Technologies, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Apr 21, 1995 |
| Received | Oct 6, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925056
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.