510(k) K955815 ยท DRX Electrode, Electrocardiograph
G3000 OR AG2000; DISPOSABLE RESTING ELECTRODE
| Applicant | Cmc Sense-It, Inc., Hopkins MN, US |
| Decision | Substantially Equivalent, Jul 23, 1996 |
| Received | Dec 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955815
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.