FDA 510(k) Application Details - K002217

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K002217
Device Name	Polymer Patient Examination Glove
Applicant	SHANGHAI CHAMPION PLASTIC PRODUCTS CO., LTD. 198 AVE. DE LA D' EMERALD SPARKS, NV 89434-9550 US Other 510(k) Applications for this Company
Contact	JANNA P TUCKER Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LZA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/24/2000
Decision Date	08/11/2000
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