510(k) K860283 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
AMI CARDIO-PAD
| Applicant | Andover Medical, Inc., Lawrence MA, US |
| Decision | Substantially Equivalent, Mar 31, 1986 |
| Received | Jan 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860283
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.