510(k) K853993 ยท DRX Electrode, Electrocardiograph
DOBE (MODIFIED)
| Applicant | Phoenix Medical Technology, Inc., Andrews SC, US |
| Decision | Substantially Equivalent, Feb 28, 1986 |
| Received | Sep 27, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853993
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.