510(k) K823048 ยท DTE Pulse-Generator, Pacemaker, External
SEA MED MODEL 880
| Applicant | Seamed Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 15, 1982 |
| Received | Oct 15, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823048
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.