510(k) K946041 ยท FMI Needle, Hypodermic, Single Lumen
CARDICO SHARPS CONTAINERS (1.5, 5, 9, 13, 21QTS.)
| Applicant | Cardico, Inc., Downey CA, US |
| Decision | Substantially Equivalent, Jun 16, 1995 |
| Received | Dec 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946041
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.