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T-SCOPE, TELEMETRIC PRECORDIAL STETHOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K894757
510(k) Type
Traditional
Applicant
LOUISVILLE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/1989
Days to Decision
53 days

T-SCOPE, TELEMETRIC PRECORDIAL STETHOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K894757
510(k) Type
Traditional
Applicant
LOUISVILLE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/1989
Days to Decision
53 days