510(k) K844911 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
ARRHYTHMIA CENTRAL-OGP-7201
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 18, 1985 |
| Received | Dec 18, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844911
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.