FDA 510(k) Applications for Medical Device Product Code "DQT"
(Occluder, Catheter Tip)

FDA 510(k) Number Applicant Device Name Decision Date
K840795 ADVANCED CARDIOVASCULAR SYSTEMS, INC. ACS SOF-T GUIDE WIREE 07/02/1984
K910339 APPLIED VASCULAR DEVICES, INC. AVD INTIMAX OCCLUSION CATHETER 05/29/1991
K983927 ARTERIAL VASCULAR ENGINEERING, INC. GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT 03/11/1999
K872790 BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC PERFUSION CATHETER 09/15/1987
K910916 CATHLAB CORP. CATHLAB SILICONE OCCLUSION BALLOON CATHETER 06/24/1991
K844918 CLINCAL INSTRUMENTS CORP. OCCLUSION & OCCLUSION-IRRIGATION 08/05/1985
K880860 DLP, INC. CORONARY OSTIUM OCCLUDER, CATALOG CODE 32015 05/26/1988
K872154 IDEAS FOR MEDICINE, INC. MODIFIED INFO INSERTS FOR PRUITT IRRI.-OCCLU. CATH 08/03/1987
K880231 IDEAS FOR MEDICINE, INC. MODIFIED PRUITT IRRIGATION & OCCLUSION CATHETER 05/25/1988
K872090 IDEAS FOR MEDICINE, INC. THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KIT 10/30/1987
K945963 MICRO INTERVENTIONAL SYSTEMS, INC. THE OMNIGUIDE GUIDING CATHETER WITH BALLOON 02/08/1995
K863559 URESIL CORP. URESIL OCCLUSION BALLOON CATHETER 10/10/1986


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