Last synced on 16 May 2025 at 11:05 pm

Electrocardiograph: SE-1200 Pro and SE-1201 Pro

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222902
510(k) Type
Traditional
Applicant
Edan Instruments, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/28/2023
Days to Decision
308 days
Submission Type
Summary

Electrocardiograph: SE-1200 Pro and SE-1201 Pro

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222902
510(k) Type
Traditional
Applicant
Edan Instruments, Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/28/2023
Days to Decision
308 days
Submission Type
Summary