FDA 510(k) Application Details - K962821

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K962821
Device Name	Anesthesia Conduction Kit
Applicant	GLOBAL MEDICAL PRODUCTS, LTD. 244 MAIN ST., SOUTH P.O. BOX 505 WOODBURY, CT 06798-0505 US Other 510(k) Applications for this Company
Contact	PETER M CLARK 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	07/19/1996
Decision Date	11/13/1996
Decision	SESK - SUBST EQUIV - KIT
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review