FDA 510(k) Applications Submitted by ANDREA RUTH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K051213	05/12/2005	PRECISION XTRA PLUS OR OPTIUM PLUS, BLOOD GLUCOSE TEST STRIPS	ABBOTT LABORATORIES INC
K030342	02/03/2003	LUMENIS FAMILY OF IPL SYSTEMS AND COMBINATION IPL/ND:YAG SYSTEMS	LUMENIS, LTD.
K040270	02/05/2004	OPUSDUO; OPUSDUO E; OPUSDUO EC; OPUS 20; OPUS SPECTRUM	LUMENIS LTD.
K030527	02/19/2003	LUMENIS FAMILY OF IPL AND COMBINATION IPL/ND:YAG SYSTEMS	LUMENIS
K010956	03/30/2001	COBRA 1/2 FLEX SURGICAL PROBE, MODEL 1593X; COBRA FLEX SURGICAL PROBE MODEL 1594X	BOSTON SCIENTIFIC CORP.
K022067	06/25/2002	CONVOY ADVANCED DELIVERY SHEATH	BOSTON SCIENTIFIC
K023291	10/02/2002	COBRA COOLED CARDIAC SURGICAL PROBE, MODEL 1596X	BOSTON SCIENTIFIC CORP.
K013349	10/09/2001	ASTRONOMER PLUS SYSTEM	EP TECHNOLOGIES, INC.
K013866	11/21/2001	CONVOY ADVANCED DELIVERY SHEATH KIT	BOSTON SCIENTIFIC
K013873	11/21/2001	COBRA CARDIAC ELECTROSURGICAL SYSTEM	BOSTON SCIENTIFIC CORP.
K181472	06/04/2018	AEROFLEX(TM) Automatic Endoscope Reprocessor with AUTOSURE(TM) MRC Monitor	Advanced Sterilization Products (ASP)