Atlas FDA

V.1 2A PROGRAMMER SOFTWARE

FDA premarket approval P880006/S033 · decided 2000-09-07

Approval details

PMA number
P880006
Supplement
S033
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
V.1 2A PROGRAMMER SOFTWARE
Generic name
Programmer, pacemaker
Applicant
St. Jude Medical, Inc.
Date received
2000-08-11
Decision date
2000-09-07
Days to decision
27 days
Decision code
APPR
Product code
KRG
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA
Statement
APPROVAL FOR THE ALTERNATE MANUFACTURING FACILITY AT INNOMEDICA, INC., MINNEAPOLIS, MN AND THE ALTERNATE STERILIZATION FACILITY AT STERIS ISOMEDIX, MINNEAPOLIS, MN.

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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