510(k) K840523 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
SERVOMED PULSE AMPLIFIER MODULE-206-
| Applicant | Litton Medical Electronics, Elk Grove Village IL, US |
| Decision | Substantially Equivalent, Oct 29, 1984 |
| Received | Feb 7, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840523
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.