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OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM814F

Page Type
Cleared 510(K)
510(k) Number
K894563
510(k) Type
Traditional
Applicant
OMRON ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1990
Days to Decision
228 days

OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM814F

Page Type
Cleared 510(K)
510(k) Number
K894563
510(k) Type
Traditional
Applicant
OMRON ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1990
Days to Decision
228 days