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ECG-1250A SERIES CARDIOFAX S AND ECG-1350A SERIES CARDIOFAX M

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072217
510(k) Type
Special
Applicant
Nihon Kohden America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2007
Days to Decision
21 days
Submission Type
Summary

ECG-1250A SERIES CARDIOFAX S AND ECG-1350A SERIES CARDIOFAX M

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072217
510(k) Type
Special
Applicant
Nihon Kohden America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2007
Days to Decision
21 days
Submission Type
Summary