510(k) K923398 ยท DTE Pulse-Generator, Pacemaker, External
CPI MODEL 2215
| Applicant | Seamed Corp., Bothell WA, US |
| Decision | Substantially Equivalent, Aug 14, 1992 |
| Received | Jul 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923398
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.