510(k) K851732 ยท DRX Electrode, Electrocardiograph
CARBOCONE
| Applicant | Imtech Corp., New York NY, US |
| Decision | Substantially Equivalent, Sep 16, 1985 |
| Received | Apr 25, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851732
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.