Last synced on 25 January 2026 at 3:41 am

Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250179
510(k) Type
Traditional
Applicant
Edan Instruments, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/29/2025
Days to Decision
188 days
Submission Type
Summary

Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250179
510(k) Type
Traditional
Applicant
Edan Instruments, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/29/2025
Days to Decision
188 days
Submission Type
Summary