Approval for the addition of an extender module to the accessory list for the generator. The extender module will allow the user to place the generator up to an additional twenty feet from the patients.
Device | THERAPY DUAL 8 CATHETER AND IBI-1500T6 CARDIAC ABLATION GENERATOR |
Classification Name | Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter |
Generic Name | Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter |
Applicant | IRVINE BIOMEDICAL,INC.(IBI) |
Date Received | 2006-08-01 |
Decision Date | 2006-09-20 |
PMA | P040042 |
Supplement | S004 |
Product Code | OAD |
Advisory Committee | Cardiovascular |
Supplement Type | Real-time Process |
Supplement Reason | Change Design/components/specifications/material |
Expedited Review | No |
Combination Product | No |
Applicant Address | IRVINE BIOMEDICAL,INC.(IBI) 2375 Morse Ave. irvine, CA 92614 |
Supplemental Filings
Supplement Number | Date | Supplement Type |
P040042 | | Original 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