510(k) K791762 ยท DTC Analyzer, Pacemaker Generator Function
SELF CHECK
| Applicant | Instromedix, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 21, 1979 |
| Received | Aug 28, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791762
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.