510(k) K880932 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
MRL PACETTE, 450SLL
| Applicant | Medical Research Laboratories, Inc., Niles IL, US |
| Decision | Substantially Equivalent, Dec 16, 1988 |
| Received | Mar 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880932
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.