510(k) K935817 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MEDSIM 300 PATIENT SIMULATOR
| Applicant | Dynatech/Nevada, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jan 18, 1994 |
| Received | Dec 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935817
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.