510(k) K850170 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
HEART AID MODEL 97
| Applicant | Cardiac Resucitator Corp., Wilsonville OR, US |
| Decision | Substantially Equivalent, Feb 14, 1985 |
| Received | Jan 16, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850170
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.