FDA 510(k) Application Details - K092411

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K092411
Device Name	Polymer Patient Examination Glove
Applicant	SHEN WEI (USA), INC. 33278 CENTRAL AVE., SUITE 102 UNION CITY, CA 94587 US Other 510(k) Applications for this Company
Contact	ALBERT LI 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	08/07/2009
Decision Date	10/21/2009
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