FDA 510(k) Application Details - K991714

Device Classification Name	Stethoscope, Electronic   More FDA Info for this Device
510(K) Number	K991714
Device Name	Stethoscope, Electronic
Applicant	DOCTOR'S RESEARCH GROUP, INC. 143 WOLCOTT RD. WOLCOTT, CT 06716 US Other 510(k) Applications for this Company
Contact	RICHARD DESLAURIERS 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	05/20/1999
Decision Date	12/10/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review