510(k) K912008 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
TRU-VIEW MULTI-CHANNEL DISPLAY
| Applicant | General Devices, Bogota NJ, US |
| Decision | Substantially Equivalent, Oct 9, 1991 |
| Received | May 6, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912008
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.