510(k) K853939 ยท DRX Electrode, Electrocardiograph
ECG-ELECTRODE(SWAROMED)
| Applicant | D. Swarovski & Co., Austria, AT |
| Decision | Substantially Equivalent, Apr 11, 1986 |
| Received | Sep 24, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853939
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.