Atlas FDA

NAVISTAR DS DIAGNOSTIC ABLATION DEFLECTABLE TIP CATHETER,

FDA premarket approval P010068/S008 · decided 2006-02-16

Approval details

PMA number
P010068
Supplement
S008
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
NAVISTAR DS DIAGNOSTIC ABLATION DEFLECTABLE TIP CATHETER,
Generic name
catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
Applicant
Biosense Webster, Inc.
Date received
2006-01-26
Decision date
2006-02-16
Days to decision
21 days
Decision code
OK30
Product code
OAD
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
CHANGE IN THE PRODUCT RELEASE.

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510(k) clearances by this applicant

RecordFirmDate
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CARTO™ 3 EP Navigation System V9.0 with PIU Plus (K254085)Biosense Webster, Inc.2026-01-18
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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
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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