FDA 510(k) Applications Submitted by DON MORRIS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K960942	02/13/1996	LATEX PATIENT EXAMINATION GLOVE	SIAM SEMPERMED CORP. LTD.
K961415	04/04/1996	LATEX PATIENT EXAMINATION GLOVE (BLUE) (MODIFICATION)	SIAM SEMPERMED CORP. LTD.
K961602	04/04/1996	LATEX PATIENT EXAMINATION GLOVE (PINK)	SIAM SEMPERMED CORP. LTD.
K981975	06/05/1998	LATEX PATIENT EXAMINATION GLOVE POWDERFREE (BLUE COLOR) POLYMER COATED	SIAM SEMPERMED CORP. LTD.
K982885	08/17/1998	PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE	SHANGHAI POSEIDON PLASTIC PRODUCTS CO., LTD.
K983612	10/14/1998	POWDER-FREE NON STERILE VINYL EXAMINATION GLOVES	SHANGHAI JIATAI PLASTIC PRODUCTS CO., LTD.