510(k) K813174 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
BRADYCARDIA ALARM
| Applicant | Douglas Scientific Products, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 22, 1982 |
| Received | Nov 6, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813174
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.