FDA 510(k) Application Details - K051171

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K051171
Device Name	Anesthesia Conduction Kit
Applicant	EPIMED INTERNATIONAL, INC. 141 SAL LANDRIO DR. CROSSROADS BUSINESS PARK JOHNSTOWN, NY 12095 US Other 510(k) Applications for this Company
Contact	CHRISTOPHER LAKE 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	05/06/2005
Decision Date	08/26/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review