510(k) K914206 ยท DPS Electrocardiograph
ARS-EKG 12K INTERPRETIVE ELECTROCARDIOGRAPHY SYST
| Applicant | Kardiosis Ltd. Co., New York NY, US |
| Decision | Substantially Equivalent, Mar 30, 1992 |
| Received | Sep 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914206
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.