FDA 510(k) Applications for Medical Device Product Code: KXF (Applicator, Absorbent Tipped, Non-Sterile)

FDA 510(k) Applications for Medical Device Product Code "KXF"
(Applicator, Absorbent Tipped, Non-Sterile)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K992553	DORMER LABORATORIES, INC.	IQ CHAMBERS	04/12/2000
K013820	EPITEST LTD. OY	FINN CHAMBER (R)	01/30/2002
K063160	SMART PRACTICE	ALLERGEAZE PATCH TEST CHAMBERS	12/22/2006
K123184	SMART PRACTICE	FINN CHAMBERS AQUA	12/19/2012
K103409	SMARTPRACTICE	ALLERGEAZE R CLEAR	03/15/2011