510(k) K963975 ยท DRX Electrode, Electrocardiograph
VERSATEC 310 ELECTRODE
| Applicant | Versatec, Inc., Bloomfield Hills MI, US |
| Decision | Substantially Equivalent, Jan 7, 1997 |
| Received | Oct 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963975
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.