510(k) K913885 ยท FMI Needle, Hypodermic, Single Lumen
RINN E-Z CAPPER
| Applicant | Rinn Corp., Elgin IL, US |
| Decision | Substantially Equivalent, Dec 13, 1991 |
| Received | Aug 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913885
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.