FDA 510(k) Application Details - K050159

Device Classification Name	Stethoscope, Electronic   More FDA Info for this Device
510(K) Number	K050159
Device Name	Stethoscope, Electronic
Applicant	3M COMPANY 3M CENTER, BLDG. 275-5W-06 ST. PAUL, MN 55133-3275 US Other 510(k) Applications for this Company
Contact	GINGER CANTOR 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	01/25/2005
Decision Date	02/22/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review