510(k) K950856 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
ZOLL PD2000 PACEMAKER/ADVISORY DEFIBRILLATOR, MODEL PD2000, ZOLL D2000 ADVISORY DEFIBRILLATOR, MODEL D2000
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent, Dec 29, 1995 |
| Received | Feb 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950856
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.