510(k) K885122 ยท FMI Needle, Hypodermic, Single Lumen
NEEDLE STICK
| Applicant | Poncy, Inc., Riviera Beach FL, US |
| Decision | Substantially Equivalent, Mar 14, 1989 |
| Received | Dec 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885122
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.