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Parker Quality & Compliance

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510(k) clearance

The Circadia CX00 System (CX00)

FDA 510(k) source

510(k) number
K262447
Applicant
Circadia Health, Inc.
Decision date
Oct 15, 2026
Date received
Jul 16, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
DRT
Device type
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Device class
Class II
Regulation
21 CFR 870.2300
Advisory committee
Cardiovascular
Statement or summary
Summary
Third party
N
Location
El Segundo, CA, US