510(k) K840353 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
PACEMAKER PULSE GENERATOR W/ELECTRODE
| Applicant | Ross Research, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 23, 1984 |
| Received | Jan 26, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840353
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.