510(k) K821673 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
HEART*AID, ALS, MODEL 95
| Applicant | Cardiac Resucitator Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 6, 1982 |
| Received | Jun 7, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821673
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.