510(k) K863514 ยท FMI Needle, Hypodermic, Single Lumen
PROMEDICOR
| Applicant | Terra Marketing Assoc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 25, 1986 |
| Received | Sep 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863514
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.