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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stethoscope, Esophageal, With Electrical Conductors
510(k) Number K823743
Device Name MODEL 40-80-2 DISPOS. ESOPHAGEAL STETHO
Applicant
Y
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
Y
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.1920
Classification Product Code
BZT  
Date Received12/13/1982
Decision Date 01/18/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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