Atlas FDA

ST JUDE MEDICAL EPIC VR/DR IMPLANTABLE CARDIOVERTER DEFIBRILLATORS (MODELS V-197 AND B-235)

FDA premarket approval P830045/S081 · decided 2002-07-30

Approval details

PMA number
P830045
Supplement
S081
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ST JUDE MEDICAL EPIC VR/DR IMPLANTABLE CARDIOVERTER DEFIBRILLATORS (MODELS V-197 AND B-235)
Generic name
Programmer, pacemaker
Applicant
St. Jude Medical, Inc.
Date received
2002-07-17
Decision date
2002-07-30
Days to decision
13 days
Decision code
APPR
Product code
KRG
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
APPROVAL FOR A DOWNSIZED VERSION OF THE PHOTON UDR/VR DEVICE. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME ST. JUDE MEDICAL EPIC VR/DR IMPLANTABLE CARDIOVERTER DEFIBRILLATORS (MODELS V-197 AND V235) AND IS INDICATED TO PROVIDE VENTRICULAR ANTITACHYCARDIA PACING AND VENTRICULAR DEFIBRILLATION FOR AUTOMATED TREATMENT OF LIFE-THREATENING VENTRICULAR ARRHYTHMIAS.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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