510(k) K961395 ยท DRX Electrode, Electrocardiograph
MEDI-TRACE RADIOLUCENT
| Applicant | Graphic Controls Corp., Buafflo NY, US |
| Decision | Substantially Equivalent, Jun 7, 1996 |
| Received | Apr 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961395
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.