510(k) K911436 ยท FMI Needle, Hypodermic, Single Lumen
SHARPS PIN CUSHION(TM) CONTAINER
| Applicant | Catalyst, Inc., Frankfort IN, US |
| Decision | Substantially Equivalent, Jul 1, 1991 |
| Received | Apr 2, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911436
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.