510(k) K960449 ยท DPS Electrocardiograph
PC ECG 1200 ECG AND STRESS ELECTROCARDIOGRAPHY TESTING SYSTEM(VERSION 2.90)
| Applicant | Biosensor Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 30, 1996 |
| Received | Jan 30, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960449
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.