510(k) K970125 ยท DRX Electrode, Electrocardiograph
NOAH MONITORING ELECTRODE SYSTEM
| Applicant | Contour Medical Technology, Inc., Lavergne TN, US |
| Decision | Substantially Equivalent, Mar 4, 1997 |
| Received | Jan 14, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970125
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.