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CARDIVAN BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K792226
510(k) Type
Traditional
Applicant
PARAMED TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1979
Days to Decision
44 days

CARDIVAN BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K792226
510(k) Type
Traditional
Applicant
PARAMED TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/1979
Days to Decision
44 days