510(k) K800935 ยท DRX Electrode, Electrocardiograph
R2 APEX-POST.,ANT.&POST. ELECT.(12 MODS)
| Applicant | R2 Corp., Walker MI, US |
| Decision | Substantially Equivalent, May 23, 1980 |
| Received | Apr 21, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800935
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.