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MODIFICATION TO: DIGITAL BLOOD PRESSURE MONITOR, MODEL 1901

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071384
510(k) Type
Traditional
Applicant
Nihon Seimitsu Sokki Co., Ltd.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/9/2007
Days to Decision
145 days
Submission Type
Summary

MODIFICATION TO: DIGITAL BLOOD PRESSURE MONITOR, MODEL 1901

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071384
510(k) Type
Traditional
Applicant
Nihon Seimitsu Sokki Co., Ltd.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/9/2007
Days to Decision
145 days
Submission Type
Summary