510(k) K860551 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
ETP 180 CARDIAC PACEMAKER (EXTERNAL)
| Applicant | Biotronics Corp., Tualatin OR, US |
| Decision | Substantially Equivalent, Apr 30, 1986 |
| Received | Feb 13, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860551
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.