510(k) K771855 ยท KRG Programmer, Pacemaker
OMNICOR PROGRAMMER MODEL 222A
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 7, 1977 |
| Received | Sep 28, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K771855
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.