FDA 510(k) Application Details - K010879

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K010879
Device Name	Latex Patient Examination Glove
Applicant	N.S. UNI-GLOVES SDN. BHD. 2420 CARSON ST. SUITE 125 TORRENCE, CA 90501 US Other 510(k) Applications for this Company
Contact	ROBERT D VANDER LEEK 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	03/23/2001
Decision Date	05/10/2001
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