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BIOSENSE WEBSTER TEMPERATURE CABLES

FDA premarket approval P950005/S008 · decided 2000-05-30

Approval details

PMA number
P950005
Supplement
S008
Supplement type
Normal 180 Day Track
Supplement reason
Express GMP Supplement
Trade name
BIOSENSE WEBSTER TEMPERATURE CABLES
Generic name
CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
Applicant
Biosense Webster, Inc.
Date received
2000-04-19
Decision date
2000-05-30
Days to decision
41 days
Decision code
APPR
Product code
DRF
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR AN ALTERNATE MANUFACTURING FACILITY LOCARTED AT BIOSENSE WEBSTER, INC., CORDIS DE MEXICO, CHIHUAHUA, MEXICO.

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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