510(k) K872778 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
PACESTART
| Applicant | Pacific Rim Engineering & Mfg., Carlsbad CA, US |
| Decision | Substantially Equivalent, Nov 4, 1987 |
| Received | Jul 14, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872778
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.