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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stethoscope, Manual
510(k) Number K905487
Device Name VARIOUS TYPES OF STETHOSCOPES
Applicant
Liaoning-Usa Corp.
123 W. Bellevue, Unit#4
Pasadena,  CA  91105
Applicant Contact JAY A BROWN
Correspondent
Liaoning-Usa Corp.
123 W. Bellevue, Unit#4
Pasadena,  CA  91105
Correspondent Contact JAY A BROWN
Regulation Number870.1875
Classification Product Code
LDE  
Date Received12/06/1990
Decision Date 04/09/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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