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OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT.

Page Type
Cleared 510(K)
510(k) Number
K930798
510(k) Type
Traditional
Applicant
OMRON HEALTHCARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/1993
Days to Decision
86 days
Submission Type
Statement

OMRON OSCILLOMETRIC DIGITAL BLOOD PRESSURE MONIT.

Page Type
Cleared 510(K)
510(k) Number
K930798
510(k) Type
Traditional
Applicant
OMRON HEALTHCARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/1993
Days to Decision
86 days
Submission Type
Statement