FDA 510(k) Application Details - K961075

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K961075
Device Name	Anesthesia Conduction Kit
Applicant	MEDCARE MEDICAL GROUP, INC. 234 OLD HOMESTEAD HWY. EAST SWANZEY, NH 03446 US Other 510(k) Applications for this Company
Contact	CRAIG J BELL Other 510(k) Applications for this Contact
Regulation Number	868.5140   More FDA Info for this Regulation Number
Classification Product Code	CAZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/18/1996
Decision Date	09/06/1996
Decision	SEKD - SUBST EQUIV - KIT WITH DRUGS
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review