510(k) K843358 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
HEART-AID MODEL 80
| Applicant | Cardiac Resucitator Corp., Wilsonville OR, US |
| Decision | Substantially Equivalent, Nov 19, 1984 |
| Received | Aug 27, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843358
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.