510(k) K234003 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
The Circadia C200 System
| Applicant | Circadia Technologies, Ltd., London, GB |
| Decision | Substantially Equivalent, May 30, 2024 |
| Received | Dec 19, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234003
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.