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DM-3000 DIGITAL BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061086
510(k) Type
Traditional
Applicant
Nihon Seimitsu Sokki Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2006
Days to Decision
114 days
Submission Type
Summary

DM-3000 DIGITAL BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061086
510(k) Type
Traditional
Applicant
Nihon Seimitsu Sokki Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2006
Days to Decision
114 days
Submission Type
Summary