Cardima, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardima, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Cardima, Inc. has 12 FDA 510(k) cleared cardiovascular devices. Based in Fremont, US.
Historical record: 12 cleared submissions from 1993 to 2006.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardima, Inc.
12 devices
Cleared
May 15, 2006
MODIFICATION TO: CARDIMA ABLATION SYSTEM
Cardiovascular
59d
Cleared
Jan 29, 2003
CARDIMA ABLATION SYSTEM
Cardiovascular
224d
Cleared
Jun 22, 1999
NAVIPORT DEFLECTABLE TIP GUIDING CATHETER
Cardiovascular
553d
Cleared
May 11, 1999
TRACER O-T-W MAPPING DEVICE
Cardiovascular
652d
Cleared
Oct 29, 1998
ELECTRODE SWITCHBOX, MODEL 11-081002
Cardiovascular
78d
Cleared
Jul 01, 1998
CARDIMA PATHFINDER 1.5F MAPPING MICROCATHETER
Cardiovascular
398d
Cleared
Jun 26, 1998
CARDIMA VUEPORT CORONARY SINUS BALLOON OCCLUSION GUIDING CATHETER
Cardiovascular
297d
Cleared
Nov 04, 1997
PATHFINDER 3MM MAPPING MICROCATHETER (01-082001)
Cardiovascular
242d
Cleared
Jan 29, 1997
PATHFINDER
Cardiovascular
404d
Cleared
Oct 05, 1995
CARDIMA, INC. FORERUNNER
Cardiovascular
181d
Cleared
Dec 21, 1993
CARDIMA TRACKER(R) INFUSION CATHETER
Cardiovascular
195d
Cleared
Sep 01, 1993
CARDIMA SEEKER AND STUBBIE GUIDEWIRES
Cardiovascular
84d