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AUTO. OSCILLOMETRIC DIGITAL BLOOD PRESS. MONITOR

Page Type
Cleared 510(K)
510(k) Number
K913523
510(k) Type
Traditional
Applicant
OMRON HEALTHCARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1991
Days to Decision
90 days
Submission Type
Statement

AUTO. OSCILLOMETRIC DIGITAL BLOOD PRESS. MONITOR

Page Type
Cleared 510(K)
510(k) Number
K913523
510(k) Type
Traditional
Applicant
OMRON HEALTHCARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1991
Days to Decision
90 days
Submission Type
Statement