510(k) K872368 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
MODIFIED VERSA STIM ELECTRODE LINE
| Applicant | Conmedcorp, Utica NY, US |
| Decision | Substantially Equivalent, Sep 18, 1987 |
| Received | Jun 18, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872368
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.