510(k) K896064 ยท DPS Electrocardiograph
AMBULATORY CARDIAC MONITOR
| Applicant | Monitech, Inc., Duluth GA, US |
| Decision | Substantially Equivalent, Jan 26, 1990 |
| Received | Oct 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896064
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.