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WRISTRECORDER CARDIAC EVENT RECORDING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K913600
510(k) Type
Traditional
Applicant
RALIN LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1991
Days to Decision
64 days
Submission Type
Statement

WRISTRECORDER CARDIAC EVENT RECORDING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K913600
510(k) Type
Traditional
Applicant
RALIN LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1991
Days to Decision
64 days
Submission Type
Statement