Atlas FDA

Celsius, Celsius RMT, EZ Steer Bi-directional non nav

FDA premarket approval P950005/S077 · decided 2021-04-07

Approval details

PMA number
P950005
Supplement
S077
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Celsius, Celsius RMT, EZ Steer Bi-directional non nav
Generic name
Cardiac ablation percutaneous catheter
Applicant
Biosense Webster, Inc.
Date received
2021-03-02
Decision date
2021-04-07
Days to decision
36 days
Decision code
APPR
Product code
LPB
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Approval for the addition of warnings from other catheter lines and the clarification of existing warnings and instructions.

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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