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Cardima, Inc.

12 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MODIFICATION TO: CARDIMA ABLATION SYSTEM (K060715)Cardima, Inc.2006-05-15
CARDIMA ABLATION SYSTEM (K022008)Cardima, Inc.2003-01-29
NAVIPORT DEFLECTABLE TIP GUIDING CATHETER (K974683)Cardima, Inc.1999-06-22
TRACER O-T-W MAPPING DEVICE (K972803)Cardima, Inc.1999-05-11
ELECTRODE SWITCHBOX, MODEL 11-081002 (K982835)Cardima, Inc.1998-10-29
CARDIMA PATHFINDER 1.5F MAPPING MICROCATHETER (K971975)Cardima, Inc.1998-07-01
CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER (K973298)Cardima, Inc.1998-06-26
PATHFINDER 3MM MAPPING MICROCATHETER (01-082001) (K970853)Cardima, Inc.1997-11-04
PATHFINDER (K955802)Cardima, Inc.1997-01-29
CARDIMA, INC. FORERUNNER (K951603)Cardima, Inc.1995-10-05
CARDIMA TRACKER(R) INFUSION CATHETER (K932800)Cardima, Inc.1993-12-21
CARDIMA SEEKER AND STUBBIE GUIDEWIRES (K932801)Cardima, Inc.1993-09-01

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Every clearance here is in the API, with alerts when new ones post.