510(k) K960264 ยท DRX Electrode, Electrocardiograph
CONMED EKG STRIPPER
| Applicant | Conmedcorp, Dayton OH, US |
| Decision | Substantially Equivalent, Apr 9, 1996 |
| Received | Jan 18, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960264
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.