510(k) K894956 ยท DPS Electrocardiograph
CIRCAMED HOLTER VERSION 4
| Applicant | Circadian, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Feb 5, 1990 |
| Received | Aug 4, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894956
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.