510(k) K915364 ยท DTE Pulse-Generator, Pacemaker, External
CHRONOCOR VI MODEL 5012
| Applicant | Seamed Corp., Bothell WA, US |
| Decision | Substantially Equivalent, Feb 7, 1992 |
| Received | Nov 27, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915364
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.