510(k) K940801 ยท DRX Electrode, Electrocardiograph
K-KLIP
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, Aug 3, 1994 |
| Received | Feb 22, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940801
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.