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EURO-DIAGNOSTIC BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904298
510(k) Type
Traditional
Applicant
MEDI-SWISS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/1991
Days to Decision
275 days

EURO-DIAGNOSTIC BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904298
510(k) Type
Traditional
Applicant
MEDI-SWISS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/1991
Days to Decision
275 days