Atlas FDA

Therapy Cool Path

FDA premarket approval P060019/S053 · decided 2021-05-18

Approval details

PMA number
P060019
Supplement
S053
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Therapy Cool Path
Generic name
catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
Applicant
Irvine Biomedical, Inc.
Date received
2021-04-19
Decision date
2021-05-18
Days to decision
29 days
Decision code
OK30
Product code
OAD
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Changes to a resin as a result of transferring resin manufacturing from the current supplier manufacturing site in LaPorte, TX to a new supplier manufacturing site in Avon, OH.

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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