FDA 510(k) Applications Submitted by SHINEMOUND ENTERPRISE, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K970625	02/19/1997	POLY-MED	SHINEMOUND ENTERPRISE, INC.
K971360	04/11/1997	SYNTEX	SHINEMOUND ENTERPRISE, INC.
K972104	06/04/1997	LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES	SHINEMOUND ENTERPRISE, INC.
K051913	07/15/2005	POWDERED LATEX PATIENT EXAMINATION GLOVES	SHINEMOUND ENTERPRISE, INC.
K993231	09/27/1999	SENSI-PRO DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES	SHINEMOUND ENTERPRISE, INC.
K993240	09/27/1999	SENSI-PRO DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES	SHINEMOUND ENTERPRISE, INC.
K994248	12/16/1999	SENSI-PRO, DISPOSABLE PRE-POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES WITH BEIGE PIGMENT ADDITIVES	SHINEMOUND ENTERPRISE, INC.
K994258	12/17/1999	SENSI-PRO DISPOSABLE POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES WITH BEIGE PIGMENT ADDITIVES	SHINEMOUND ENTERPRISE, INC.