510(k) K852469 ยท DRX Electrode, Electrocardiograph
SAF-D-FIB
| Applicant | Medtronic Andover Medical, Inc., Lowell MA, US |
| Decision | Substantially Equivalent, Sep 16, 1985 |
| Received | Jun 13, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852469
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.