510(k) K830830 ยท DSI Detector And Alarm, Arrhythmia
CIRCA MED TWO-CHANNEL
| Applicant | Circadian, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 18, 1983 |
| Received | Mar 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830830
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.