FDA 510(k) Applications for Medical Device Product Code: EKR (Plugger, Root Canal, Endodontic)

FDA 510(k) Applications for Medical Device Product Code "EKR"
(Plugger, Root Canal, Endodontic)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K060347	B&L BIOTECH CO., LTD.	B&L L-BETA, MODEL WL-B1	06/05/2006
K031664	SYBRON ENDO/ANALYTIC	ELEMENTS OBTURATION UNIT	04/28/2004
K042828	YOUNG O/S LLC	OBTURA GUTTA PERCHA DELIVERY SYSTEM, MODEL 823-700	12/01/2004