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THERAPY CARDIAC ABLATION CATHETERS

FDA premarket approval P040014/S008 · decided 2009-06-17

Approval details

PMA number
P040014
Supplement
S008
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
THERAPY CARDIAC ABLATION CATHETERS
Generic name
Cardiac ablation percutaneous catheter
Applicant
Irvine Biomedical, Inc.
Date received
2008-09-04
Decision date
2009-06-17
Days to decision
286 days
Decision code
APPR
Product code
LPB
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR SOFTWARE CHANGES IN THE IBI 1500T9 RF GENERATOR WITH SOFTWARE VERSION 1.42.

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510(k) clearances by this applicant

RecordFirmDate
INQUIRY H-CURVE TV STEERABLE DIAGNOSTIC CATHETER (K082061)Irvine Biomedical, Inc.2008-08-19
INQUIRY OPTIMA PLUS STEERABLE ELECTROPHYSIOLOGY CATHETER (K060757)Irvine Biomedical, Inc.2006-04-19
INQUIRY AFOCUS II DIAGNOSTIC CATHETER (K053582)Irvine Biomedical, Inc.2006-03-21
INQUIRY AFOCUS, INQUIRY AFOCUS II AND INQUIRY OPTIMA STEERABLE ELECTROPHYSIOLOGY CATHETER (K042775)Irvine Biomedical, Inc.2004-11-04
AFOCUS ELECTROPYSIOLOGY CATHETER SYSTEM, MODELS 81550, 81567, 81568, 81569 (K010471)Irvine Biomedical, Inc.2001-06-06
LUMA-CATH STEERABLE EP CATHETERS (K991878)Irvine Biomedical, Inc.1999-12-10
LUMA-CATH FIXED CURVE EP CATHETERS (K991025)Irvine Biomedical, Inc.1999-10-15
ORTHOGONAL EP CATHETERS (K990958)Irvine Biomedical, Inc.1999-06-03