510(k) K831878 ยท DPS Electrocardiograph
CARDIO-SCOPE MINI MONITOR
| Applicant | W.E. Leder Enterprises, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 29, 1983 |
| Received | Jun 13, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831878
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.