FDA 510(k) Applications Submitted by SHANGHAI CHINASTAR CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K010247	01/26/2001	SHANGHAI CHINASTAR POWER-FREE BLUE NITRIL EXAMINATION GLOVES	SHANGHAI CHINASTAR CORP.
K003675	11/29/2000	SHANGHAI CHINA STAR CORP POWDERED BLUE NITRILE PATIENT EXAMINATION GLOVES	SHANGHAI CHINASTAR CORP.
K992205	06/30/1999	PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES	SHANGHAI CHINASTAR CORP.
K992206	06/30/1999	POWDER-FREE VINYL PATIENT EXAMINATION GLOVES	SHANGHAI CHINASTAR CORP.