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ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014204
510(k) Type
Traditional
Applicant
K-Jump Health Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2002
Days to Decision
74 days
Submission Type
Summary

ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K014204
510(k) Type
Traditional
Applicant
K-Jump Health Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2002
Days to Decision
74 days
Submission Type
Summary