510(k) K924820 ยท FMI Needle, Hypodermic, Single Lumen
HYPOGRIP(TM)
| Applicant | Collett Products, Boise ID, US |
| Decision | Substantially Equivalent, Oct 5, 1993 |
| Received | Sep 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924820
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.