510(k) K871971 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
MODIFIED PACE*AID MODEL 53
| Applicant | Cardiac Resucitator Corp., Portland OR, US |
| Decision | Substantially Equivalent, Jun 24, 1987 |
| Received | May 21, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871971
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.