510(k) K894991 ยท DRX Electrode, Electrocardiograph
ELECTRO BLUE ECG ELECT. FOAM, SILVER/SILVER CHLO.
| Applicant | Labeltape Meditect, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Oct 26, 1989 |
| Received | Aug 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894991
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.