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VASOSEAL 4-5 FRENCH SYSTEM

FDA premarket approval P920004/S017 · decided 2002-06-11

Approval details

PMA number
P920004
Supplement
S017
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
VASOSEAL 4-5 FRENCH SYSTEM
Generic name
Device, hemostasis, vascular
Applicant
St. Jude Medical, Inc.
Date received
2002-02-14
Decision date
2002-06-11
Days to decision
117 days
Decision code
APPR
Product code
MGB
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
APPROVAL TO MARKET A SMALLER VERSION OF THE VASOSEAL VHD DEVICE. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME VASOSEAL 4-5 FRENCH SYSTEM AND IS INDICATED FOR "USE IN SEALING THE FEMORAL ARTERIAL PUNCTURE SITE IN PATIENTS WHO HAVE UNDERGONE DIAGNOSTIC CATHETERIZATION PROCEDURES USING A 4 OR 5 FRENCH PROCEDURAL SHEATH AND USING A RETROGRADE APPROACH. THE VASOSEAL 4-5 FRENCH SYSTEM REDUCES TIME TO HEMOSTASIS, AMBULATION AND DISCHARGE IN PATIENTS WHO HAVE UNDERGONE DIAGNOSTIC CATHE

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510(k) clearances by this applicant

RecordFirmDate
Advisor HD Grid Mapping Catheter, Sensor Enabled (K172393)St. Jude Medical, Inc.2018-04-23
Confirm Rx Insertable Cardiac Monitor (ICM) System (K163407)St. Jude Medical, Inc.2017-09-29
PressureWire X Guidewire (K161171)St. Jude Medical, Inc.2016-08-15
Nanostim Introducer Kit (K161102)St. Jude Medical, Inc.2016-05-19
The Nanostim Introducer Kit (K160716)St. Jude Medical, Inc.2016-04-14
NANOSTIM INTRODUCER KIT (K140793)St. Jude Medical, Inc.2014-12-17
SJM CONFIRM IMPLANTABLE CARDIAC MONITOR (ICM) (K133481)St. Jude Medical, Inc.2014-05-28
ENLIGHTN RENAL GUIDE CATHETER (K131592)St. Jude Medical, Inc.2014-01-31