FDA 510(k) Application Details - K081971

Device Classification Name	Patient Examination Glove, Specialty   More FDA Info for this Device
510(K) Number	K081971
Device Name	Patient Examination Glove, Specialty
Applicant	NITRITEX (M) SDN. BHD. KEBUN BARU, JLN MASJID TELOK PANGLIMA GARANG KUALA LANGAT, SELANGOR DE 42500 MY Other 510(k) Applications for this Company
Contact	DEREK WATTS Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LZC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/10/2008
Decision Date	12/23/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review