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OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881601
510(k) Type
Traditional
Applicant
OMRON TATEISI ELECTRONICS CO.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
6/15/1988
Days to Decision
63 days

OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881601
510(k) Type
Traditional
Applicant
OMRON TATEISI ELECTRONICS CO.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
6/15/1988
Days to Decision
63 days