510(k) K901031 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PCI MODEL 2041-PC TELEMETRY MONITOR
| Applicant | Accucore, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, May 17, 1990 |
| Received | Mar 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901031
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.