510(k) K960968 ยท DRX Electrode, Electrocardiograph
MEDI-TRACE 200, MEDI-TRACE 200-30
| Applicant | Graphic Controls Corp., Buafflo NY, US |
| Decision | Substantially Equivalent, Oct 28, 1996 |
| Received | Mar 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960968
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.