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MODEL WS-500 DIGITAL WRIST BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003444
510(k) Type
Traditional
Applicant
Nihon Seimitsu Sokki Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2000
Days to Decision
15 days
Submission Type
Summary

MODEL WS-500 DIGITAL WRIST BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003444
510(k) Type
Traditional
Applicant
Nihon Seimitsu Sokki Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2000
Days to Decision
15 days
Submission Type
Summary