FDA 510(k) Application Details - K052214

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K052214
Device Name	Latex Patient Examination Glove
Applicant	KANAM LATEX INDUSTRIES PVT. LTD. OOPPOOTTIL BUILDING P.O. BOX #28K.K. ROAD KOTTAYAM, KERALA 686001 IN Other 510(k) Applications for this Company
Contact	RAVI ABRAHAM Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LYY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/15/2005
Decision Date	09/13/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review