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OMRON INTELLISENSE DIGITAL BLOOD PRESSURE MONITOR, MODEL HEM-907XL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032305
510(k) Type
Traditional
Applicant
Omron Healthcare, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2004
Days to Decision
201 days
Submission Type
Statement

OMRON INTELLISENSE DIGITAL BLOOD PRESSURE MONITOR, MODEL HEM-907XL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032305
510(k) Type
Traditional
Applicant
Omron Healthcare, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2004
Days to Decision
201 days
Submission Type
Statement