510(k) K780209 ยท FMI Needle, Hypodermic, Single Lumen
DILUTION SPIKE
| Applicant | Sterling Drug, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 10, 1978 |
| Received | Feb 6, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780209
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.