FDA 510(k) Applications for Medical Device Product Code: NKX (Needle, Phacoemulsification, Reprocessed)

FDA 510(k) Applications for Medical Device Product Code "NKX"
(Needle, Phacoemulsification, Reprocessed)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K060648	ALLIANCE MEDICAL CORP.	REPROCESSED PHACOEMULSIFICATION TIPS	03/19/2007
K050518	ALLIANCE MEDICAL, INC.	REPROCESSED PHACOEMUISIFICATION TIPS	09/23/2005
K012579	STERILMED, INC.	REPROCESSED PHACO TIPS	11/08/2001
K030179	SURGICAL INSTRUMENTS SERVICE AND SAVINGS, INC.	MEDISISS PHACOEMULSIFICATION TIPS/NEEDLES	01/24/2003
K012698	VANGUARD MEDICAL CONCEPTS, INC.	VANGUARD REPROCESSED PHACOEMULSIFICATION	11/09/2001