FDA 510(k) Application Details - K961848

Device Classification Name	Stethoscope, Electronic   More FDA Info for this Device
510(K) Number	K961848
Device Name	Stethoscope, Electronic
Applicant	MINNESOTA MINING AND MFG. CO. 3M CENTER, BUILDING 275-3E-08 P.O. BOX 33275 ST. PAUL, MN 55133-3275 US Other 510(k) Applications for this Company
Contact	LINDA JONSEN 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	05/13/1996
Decision Date	09/26/1997
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