510(k) K820609 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
HEART *AID, #80
| Applicant | Cardiac Resucitator Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 6, 1982 |
| Received | Mar 8, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820609
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.