510(k) K840569 ยท DPS Electrocardiograph
EKG 501 A
| Applicant | Bosch Hearing Instruments, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 30, 1985 |
| Received | Feb 8, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840569
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.