510(k) K000660 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413
| Applicant | Medical Data Electronics, Arleta CA, US |
| Decision | Substantially Equivalent, Mar 28, 2000 |
| Received | Feb 28, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000660
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.