THERAPY DUAL 8 CATHETER AND IBI-1500T6 CARDIAC ABLATION GENERATOR

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Premarket Approval P040042 S006

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Approval for 1) the addition of thermistor temperature sensor catheters to the therapy catheter model mix, 2) the addition of a 1763-e compatible interface cable to the 4mm thermistor ablation catheter, and 3) the addition of the 1778-e compatible interface cable to the 8mm thermistor ablation catheter.

DeviceTHERAPY DUAL 8 CATHETER AND IBI-1500T6 CARDIAC ABLATION GENERATOR
Classification NameCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
Generic NameCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
ApplicantIRVINE BIOMEDICAL,INC.(IBI)
Date Received2006-09-05
Decision Date2007-01-10
PMAP040042
SupplementS006
Product CodeOAD
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address IRVINE BIOMEDICAL,INC.(IBI) 2375 Morse Ave. irvine, CA 92614

Supplemental Filings

Supplement NumberDateSupplement Type
P040042Original Filing
S054 2022-11-14 30-day Notice
S053
S052 2022-10-19 Normal 180 Day Track No User Fee
S051 2021-09-14 30-day Notice
S050 2021-04-13 30-day Notice
S049 2021-02-25 30-day Notice
S048 2021-01-13 Real-time Process
S047 2020-09-18 30-day Notice
S046
S045 2020-02-20 Real-time Process
S044 2020-02-04 30-day Notice
S043 2019-07-29 30-day Notice
S042 2019-03-15 30-day Notice
S041 2018-12-12 Special (immediate Track)
S040 2018-02-05 30-day Notice
S039
S038
S037 2017-05-04 30-day Notice
S036 2016-08-12 30-day Notice
S035 2016-05-27 30-day Notice
S034 2016-02-19 30-day Notice
S033 2015-11-20 Real-time Process
S032 2015-09-23 30-day Notice
S031 2015-08-21 Normal 180 Day Track No User Fee
S030 2015-04-20 30-day Notice
S029 2014-11-07 Real-time Process
S028 2014-04-30 Normal 180 Day Track No User Fee
S027 2014-03-03 Real-time Process
S026 2013-11-27 Normal 180 Day Track
S025 2013-08-30 30-day Notice
S024 2011-11-29 135 Review Track For 30-day Notice
S023 2011-10-14 30-day Notice
S022 2011-05-09 30-day Notice
S021 2011-01-18 30-day Notice
S020 2010-11-16 Real-time Process
S019
S018 2010-02-22 30-day Notice
S017 2009-12-14 30-day Notice
S016 2009-07-30 30-day Notice
S015 2009-05-04 30-day Notice
S014 2008-11-10 30-day Notice
S013 2008-09-04 Normal 180 Day Track
S012 2008-05-14 30-day Notice
S011 2007-09-19 30-day Notice
S010 2007-03-16 30-day Notice
S009 2007-03-12 Normal 180 Day Track
S008 2007-02-12 Real-time Process
S007 2006-12-18 135 Review Track For 30-day Notice
S006 2006-09-05 Normal 180 Day Track
S005 2006-08-18 Real-time Process
S004 2006-08-01 Real-time Process
S003 2006-06-02 Real-time Process
S002 2006-05-01 Real-time Process
S001 2005-11-22 30-day Notice

NIH GUDID Devices

Device IDPMASupp
05414734306980 P040042 000
05414734306973 P040042 000
05414734306997 P040042 000
05414734307000 P040042 000
05414734307024 P040042 000
05414734307017 P040042 000
05414734308939 P040042 005
05414734309073 P040042 006
05414734307550 P040042 006
05414734307567 P040042 006
05414734307581 P040042 006
05414734307598 P040042 006
05414734300162 P040042 009
05414734300179 P040042 009
05414734300186 P040042 009
05414734300193 P040042 009
05414734300247 P040042 009
05414734300254 P040042 009
05414734300261 P040042 009
05414734300278 P040042 009
05414734300155 P040042 009

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