FDA 510(k) Applications Submitted by ALLYSON BARFORD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040827	03/30/2004	PANALOK LOOP ANCHOR	DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K041064	04/23/2004	BIOKNOTLESS RC ANCHOR	Depuy Mitek
K041065	04/23/2004	PANALOK RC LOOP ANCHOR	Depuy Mitek
K041115	04/29/2004	GII QUICKANCHOR PLUS	DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K041116	04/29/2004	SUPER QUICKANCHOR PLUS	Depuy Mitek
K041117	04/29/2004	PANALOK RC QUICKANCHOR PLUS, MODEL 212130, 212730; DUAL SUTURE PANALOK RC QUICKANCHOR PLLUS, MODELS 212132, 212732	Depuy Mitek
K061231	05/02/2006	WELLFLEX BILIARY RX STENT SYSTEM	BOSTON SCIENTIFIC CORP.
K052194	08/11/2005	SPYGLASS DIRECT VISUALIZATION PROBE AND OCULAR	BOSTON SCIENTIFIC CORP.
K062750	09/14/2006	WALLFLEX ENTERAL DUODENAL STENT WITH ANCHOR LOCK DELIVERY SYSTEM, MODELS M00565010, M00565020, M00565030	BOSTON SCIENTIFIC CORP.