FDA 510(k) Application Details - K083903

Device Classification Name	Stethoscope, Electronic   More FDA Info for this Device
510(K) Number	K083903
Device Name	Stethoscope, Electronic
Applicant	3M COMPANY 3M CENTER, BLDG. 275-5W-06 ST. PAUL, MN 55144-1000 US Other 510(k) Applications for this Company
Contact	JIZHONG JIN Other 510(k) Applications for this Contact
Regulation Number	870.1875   More FDA Info for this Regulation Number
Classification Product Code	DQD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/29/2008
Decision Date	07/15/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review