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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name transmitters and receivers, physiological signal, radiofrequency
510(k) Number K120704
Device Name 3M LITTMANN TELESTETH ONLINE AUSCULATION SYSTEM
Original Applicant
3M COMPANY
3m center, bldg. 275-5w-06
st. paul,  MN  55133 3275
Original Contact jon platt
Regulation Number870.2910
Classification Product Code
DRG  
Date Received03/08/2012
Decision Date 05/03/2012
Decision substantially equivalent (SE)
Classification Advisory Committee Cardiovascular
Review Advisory Committee Cardiovascular
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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