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CARDIODYNE KINETORR/PC BLOOD PRESSURE MONITORS

Page Type
Cleared 510(K)
510(k) Number
K911871
510(k) Type
Traditional
Applicant
CARDIODYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1991
Days to Decision
195 days
Submission Type
Statement

CARDIODYNE KINETORR/PC BLOOD PRESSURE MONITORS

Page Type
Cleared 510(K)
510(k) Number
K911871
510(k) Type
Traditional
Applicant
CARDIODYNE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1991
Days to Decision
195 days
Submission Type
Statement