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SE-601 SERIES ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090367
510(k) Type
Traditional
Applicant
Edan Instruments, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2009
Days to Decision
110 days
Submission Type
Summary

SE-601 SERIES ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090367
510(k) Type
Traditional
Applicant
Edan Instruments, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2009
Days to Decision
110 days
Submission Type
Summary