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WRISTRECORDER CARDIAC EVENT RECORDING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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