510(k) K791379 ยท DXY Implantable Pacemaker Pulse-Generator
MODEL 228-02 THINLITH II PACEMAKER, BIPO
| Applicant | Intermedics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 12, 1979 |
| Received | Jul 24, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791379
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.