FDA 510(k) Applications for Medical Device Product Code: LWI (Ultrasound, Sinus)

FDA 510(k) Applications for Medical Device Product Code "LWI"
(Ultrasound, Sinus)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K960241	CUSTOM PACK RELIABILITY	CPR GENERAL SURGERY TRAY	03/22/1996
K960044	ENTLAB OY	ULTRAMAX/MODEL NUMBER A1	08/02/1996
K960421	FERGUSON MEDICAL	SINUSCAN 102/SINUSPRINT	04/16/1997

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