510(k) K831381 ยท DTE Pulse-Generator, Pacemaker, External
RAPID ATRIAL PACER
| Applicant | Seamed Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 31, 1983 |
| Received | Apr 28, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831381
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.