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The Circadia C200 System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234003
510(k) Type
Traditional
Applicant
Circadia Technologies, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/30/2024
Days to Decision
163 days
Submission Type
Summary

The Circadia C200 System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234003
510(k) Type
Traditional
Applicant
Circadia Technologies, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/30/2024
Days to Decision
163 days
Submission Type
Summary