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MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030221
510(k) Type
Traditional
Applicant
Mytech Technology Co., Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
7/25/2003
Days to Decision
185 days
Submission Type
Statement

MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030221
510(k) Type
Traditional
Applicant
Mytech Technology Co., Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
7/25/2003
Days to Decision
185 days
Submission Type
Statement