510(k) K884530 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
TRIAD-EP II, PLATE INPUT
| Applicant | Cardiotronics, Inc., West Carlsbad CA, US |
| Decision | Substantially Equivalent, Nov 17, 1988 |
| Received | Oct 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884530
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.