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KENZ ECG 108 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS; KENZ ECG 110 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS WITH EC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001896
510(k) Type
Traditional
Applicant
SUZUKEN CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2001
Days to Decision
201 days
Submission Type
Summary

KENZ ECG 108 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS; KENZ ECG 110 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS WITH EC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001896
510(k) Type
Traditional
Applicant
SUZUKEN CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2001
Days to Decision
201 days
Submission Type
Summary