FDA 510(k) Applications for Medical Device Product Code: NMF (Clamp, Vascular, Reprocessed)

FDA 510(k) Applications for Medical Device Product Code "NMF"
(Clamp, Vascular, Reprocessed)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K120204	STERILMED, INC.	REPROCESSED FEMORAL COMPRESSION DEVICE	04/03/2012
K012574	STERILMED, INC.	REPROCESSED FEMORAL COMPRESSION DEVICE	07/18/2002
K011832	VANGUARD MEDICAL CONCEPTS, INC.	VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE	12/21/2001