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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name stethoscope, electronic
510(k) Number K041934
FOIA Releasable 510(k) K041934
Device Name 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000
Applicant
3M COMPANY
3M CENTER, BLDG. 275-5W-06
ST. PAUL,  MN  55144 -1000
Applicant Contact GINGER CANTOR
Correspondent
3M COMPANY
3M CENTER, BLDG. 275-5W-06
ST. PAUL,  MN  55144 -1000
Correspondent Contact GINGER CANTOR
Regulation Number870.1875
Classification Product Code
DQD  
Date Received07/19/2004
Decision Date 10/15/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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