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NAVISTAR DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER

FDA premarket approval P990025/S008 · decided 2003-02-04

Approval details

PMA number
P990025
Supplement
S008
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
NAVISTAR DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER
Generic name
CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
Applicant
Biosense Webster, Inc.
Date received
2003-01-02
Decision date
2003-02-04
Days to decision
33 days
Decision code
APPR
Product code
DRF
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR ESTABLISHING AND EXTENDING PACKAGE AND PRODUCT SHELF LIVES.

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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