510(k) K792096 ยท FMI Needle, Hypodermic, Single Lumen
2 FR KELMAN CHAMBER MAINTAINER
| Applicant | Heyer Schulte Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 16, 1979 |
| Received | Oct 18, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792096
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.