510(k) K896569 ยท DRX Electrode, Electrocardiograph
ELECTROTRACE DISPOSABLE AG/AGCL EKG MONITOR ELEC.
| Applicant | Jason Marketing Co., Huntington Beach CA, US |
| Decision | Substantially Equivalent, Jan 18, 1990 |
| Received | Nov 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896569
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.