510(k) K834600 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
RECOMB ECG PREAMPLIFIER/206 069 03
| Applicant | Litton Medical Electronics, Walker MI, US |
| Decision | Substantially Equivalent, Jun 1, 1984 |
| Received | Dec 30, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834600
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.