FDA 510(k) Applications Submitted by Dynarex Corporation

FDA 510(k) Number	Submission Date	Device Name	Applicant
K092488	08/13/2009	DYNAREX STERILE LUBRICATING JELLY	DYNAREX CORPORATION
K102637	09/14/2010	DYNAREX ULTRASOUND GEL	DYNAREX CORPORATION
K103086	10/19/2010	DYNAREX INTERMITTENT CATHETERS, MALE, FEMALE, PEDIATRIC	DYNAREX CORPORATION
K151575	06/11/2015	Dynarex Eye Cups	DYNAREX CORPORATION
K082863	09/29/2008	DYNAREX ENTERAL DELIVERY PUMP SET WITH SPIKE (1000ML), DYNAREX ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE (1000ML)	DYNAREX CORPORATION
K152970	10/08/2015	Dynarex Xeroform Petrolatum Dressing	DYNAREX CORPORATION
K172266	07/27/2017	Dynarex Three-Way Stopcock	Dynarex Corporation
K081569	06/04/2008	DYNAREX/TILLOTSON NON-STERILE POWDER FREE BLUE NITRILE PATIENT EXAM GLOVE FOR USE WITH CHEMOTHERAPY DRUGS	DYNAREX CORPORATION