510(k) K884139 ยท FMI Needle, Hypodermic, Single Lumen
ACCI-GUARD(TM) REGULAR AND PEDIATRIC HOLDER
| Applicant | Medical Safety Products, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Oct 6, 1988 |
| Received | Sep 30, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884139
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.