Last synced on 25 January 2026 at 3:41 am

Patient Monitor (iX10, iX12, iX15)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232962
510(k) Type
Traditional
Applicant
Edan Instruments, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/19/2024
Days to Decision
211 days
Submission Type
Summary

Patient Monitor (iX10, iX12, iX15)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232962
510(k) Type
Traditional
Applicant
Edan Instruments, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/19/2024
Days to Decision
211 days
Submission Type
Summary