510(k) K934000 ยท DRX Electrode, Electrocardiograph
SENTRY AQUEOUS GEL ECG ELECTRODES
| Applicant | Sentry Medical Products, Inc., Lombard IL, US |
| Decision | Substantially Equivalent, Aug 30, 1994 |
| Received | Aug 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934000
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.