510(k) K850791 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
MDI 2000 - PULSE GENERATOR
| Applicant | Micromedical Devices, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Jun 19, 1985 |
| Received | Feb 26, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850791
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.