FDA 510(k) Applications Submitted by LATEXX PARTNERS BHD.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K992671	08/10/1999	QTEXX PRE-POWDERED NITRILE EXAMINATION GLOVES	LATEXX PARTNERS BHD.
K991462	04/27/1999	QTEXX POWDER FREE LATEX EXAMINATION GLOVES, POLYMER COATED	LATEXX PARTNERS BHD.
K011791	06/08/2001	POWDER FREE NITRILE EXAMINATION GLOVES, VIOLET COLOR	LATEXX PARTNERS BHD.
K011792	06/08/2001	NON-CHLORINATED, POLYMER COATED POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES	LATEXX PARTNERS BHD.
K981159	03/31/1998	PROFLEX POWDER FREE NITRILE EXAMINATION GLOVES	LATEXX PARTNERS BHD.
K981767	05/19/1998	QTEXX POWDERFREE LATEX EXAMINATION GLOVES	LATEXX PARTNERS BHD.
K992924	08/30/1999	QTEXX, NON-CHLORINATED, POWDER FREE NITRILE EXAMINATION GLOVES, POLYMER-COATED	LATEXX PARTNERS BHD.