510(k) K890473 ยท FMI Needle, Hypodermic, Single Lumen
NEEDLE GUARD(TM)
| Applicant | Martech Medical Products, Inc., Riverside CA, US |
| Decision | Substantially Equivalent, Apr 3, 1989 |
| Received | Jan 31, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890473
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.