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VARIPULSE (TM) Catheter; TRUPULSE (TM) Generator; Sterile Interface Cable; nGEN (TM) Pump

FDA premarket approval P240006/S001 · decided 2025-05-09

Approval details

PMA number
P240006
Supplement
S001
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
VARIPULSE (TM) Catheter; TRUPULSE (TM) Generator; Sterile Interface Cable; nGEN (TM) Pump
Generic name
Percutaneous Cardiac Ablation Catheter for Treatment of Atrial Fibrillation with Irreversible Electroporation
Applicant
Biosense Webster, Inc.
Date received
2024-12-06
Decision date
2025-05-09
Days to decision
154 days
Decision code
APPR
Product code
QZI
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
approval of the protocol for the post-approval study (PAS) submitted to comply with the conditions of approval outlined in our approval order for P240006 dated November 6, 2024.

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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