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GE Medical Systems Information Technologies

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
GE Healthcare Centricity Cardiology AI1000 Workstation version 4.2.6 and version 4.2.7.05 recall (Z-1421-05)GE Medical Systems Information Technologies2005-08-30
Dinalink brand Communication Cable which is an accessory to a medical device Dinalike whic recall (Z-1015-04)GE Medical Systems Information Technologies2004-07-20
Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAM recall (Z-0011-04)GE Medical Systems Information Technologies2003-10-15
Critikon brand Omni-Stat Finger Sensor - P/N 009084 recall (Z-0013-04)GE Medical Systems Information Technologies2003-10-15
Critikon brand Omni-Sat Neonatal, Semi-Disposable Sensor, P/N 009130 recall (Z-0014-04)GE Medical Systems Information Technologies2003-10-15
Critikon brand Omni-Sat Adult, Semi-Disposable Sensor - P/N 009136 recall (Z-0015-04)GE Medical Systems Information Technologies2003-10-15
Infant reusable blood pressure cuffs, one tube, male slip luer connector, P/N 2930 , manuf recall (Z-1237-03)GE Medical Systems Information Technologies2003-10-15
GE Medical Systems COROMETRICS Maternal/Fetal Monitoring Systems, Models 2126is, 2128is, 2 recall (Z-1291-03)GE Medical Systems Information Technologies2003-09-23
Critikon brand Adult, DURA-CUF, product code 2790, used as an arm cuff in association with recall (Z-1236-03)GE Medical Systems Information Technologies2003-09-17

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Every clearance here is in the API, with alerts when new ones post.