510(k) K800243 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
D668 & D664 CENTRAL MONITORING SYSTEMS
| Applicant | Medtel Pty. , Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 10, 1980 |
| Received | Feb 5, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800243
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.