FDA 510(k) Applications for Medical Device Product Code: OXD ()

FDA 510(k) Applications for Medical Device Product Code "OXD"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K010936	W.L. GORE & ASSOCIATES,INC	MODIFICATION TO SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL	05/21/2001
K001789	W.L. GORE & ASSOCIATES,INC	SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL	07/06/2000
K955364	W.L. GORE & ASSOCIATES,INC	SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL	02/01/1996