510(k) K770328 ยท DXY Implantable Pacemaker Pulse-Generator
PACEMAKER, ANTRIO-VENTRICULAR SEQ.
| Applicant | American Pacemaker Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 28, 1977 |
| Received | Feb 17, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770328
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.