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EZ STEER THERMOCOOL NAV CATHETER

FDA premarket approval P030031/S022 · decided 2010-07-07

Approval details

PMA number
P030031
Supplement
S022
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
EZ STEER THERMOCOOL NAV CATHETER
Generic name
Cardiac ablation percutaneous catheter
Applicant
Biosense Webster, Inc.
Date received
2009-11-17
Decision date
2010-07-07
Days to decision
232 days
Decision code
APPR
Product code
LPB
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR MODIFICATIONS TO THE CATHETERS TO MAKE THEM COMPATIBLE WITH THE CARTO 3 ELECTROANATOMIC NAVIGATION SYSTEM, AND THE ADDITION OF TWO RING ELECTRODES FOR SHAFT VISUALIZATION ON CARTO 3.

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510(k) clearances by this applicant

RecordFirmDate
CARTO™ 3 EP Navigation System V8.4 (K252972)Biosense Webster, Inc.2026-02-20
CARTO™ 3 EP Navigation System V9.0 with PIU Plus (K254085)Biosense Webster, Inc.2026-01-18
CARTO™ 3 EP Navigation System V8.1 (K252302)Biosense Webster, Inc.2025-08-22
NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter (K241540)Biosense Webster, Inc.2024-06-28
SOUNDSTAR™ CRYSTAL Ultrasound Catheter (K240050)Biosense Webster, Inc.2024-06-12
CARTO™ 3 EP Navigation System Software V8.0 (FG-5400-00, FG-5400-00U) (K231207)Biosense Webster, Inc.2023-09-07
PENTARAY® NAV ECO High Density Mapping Catheter, DECANAV® Mapping Catheter, Webster® CS Catheter with Auto ID, Webster® CS Catheter with EZ Steer Technology, Webster® CS Catheter with EZ Steer Technology with Auto ID (K231312)Biosense Webster, Inc.2023-07-10
CARTO VIZIGO® 8.5F Bi-Directional Guiding Sheath (D-1385-01-S, D-1385-02-S, D-1385-03-S) (K231412)Biosense Webster, Inc.2023-07-10