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THERAPY ABLATION CATHETERS

FDA premarket approval P040014/S027 · decided 2015-10-21

Approval details

PMA number
P040014
Supplement
S027
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
THERAPY ABLATION CATHETERS
Generic name
Cardiac ablation percutaneous catheter
Applicant
Irvine Biomedical, Inc.
Date received
2015-09-23
Decision date
2015-10-21
Days to decision
28 days
Decision code
OK30
Product code
LPB
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
TO REMOVE A REDUNDANT RUN-IN TEST FOR THE AMPERE SYSTEM FROM THE MANUFACTURING PROCESS.

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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