510(k) K962122 ยท DRX Electrode, Electrocardiograph
SENTRY RADIOTRANSLUCENT ECG ELECTRODES
| Applicant | Sentry Medical Products, Inc., Lombard IL, US |
| Decision | Substantially Equivalent, Jul 24, 1996 |
| Received | May 31, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962122
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.