510(k) K180873 ยท DTE Pulse-Generator, Pacemaker, External
Medtronic Model 53401 External Pulse Generator (EPG)
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Apr 19, 2018 |
| Received | Apr 3, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180873
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.