510(k) K821003 ยท DXY Implantable Pacemaker Pulse-Generator
PROGRAMMALITH II, #225 & 226
| Applicant | Pacesetter Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, May 7, 1982 |
| Received | Apr 9, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821003
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.