Atlas FDA

DISCOVERY MR750 3.0T ,DISCOVERY MR450 1.5T, DISCOVERY MR750 3.0T,OPTIMA MR450W 1.5T

FDA 510(k) clearance K142085 · decided 2014-09-26

Clearance details

K-number
K142085
Device name
DISCOVERY MR750 3.0T ,DISCOVERY MR450 1.5T, DISCOVERY MR750 3.0T,OPTIMA MR450W 1.5T
Applicant
Ge Medical Systems, LLC
Decision
Substantially Equivalent
Date received
2014-07-31
Decision date
2014-09-26
Days to decision
57 days
Clearance type
Traditional
Product code
LNH
Device class
2
Regulation number
892.1000
Medical specialty
Radiology
Advisory committee
Radiology
Location
Waukesha, WI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
GE Discovery MR450 1.5T, Nuclear Magnetic Resonance Imaging System recall (Z-2301-2025)GE Medical Systems, LLC2025-08-13
GE Optima MR450w 1.5T, Nuclear Magnetic Resonance Imaging System recall (Z-2302-2025)GE Medical Systems, LLC2025-08-13
GE Discovery MR750 3.0T, Nuclear Magnetic Resonance Imaging System recall (Z-2306-2025)GE Medical Systems, LLC2025-08-13
Discovery MR750w 3.0T, whole body magnetic resonance scanner recall (Z-0517-2025)GE Medical Systems, LLC2024-11-22
Discovery MR750 3.0T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0 to D recall (Z-2464-2024)GE Medical Systems, LLC2024-08-02
Discovery MR750w 3.0T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0 to recall (Z-2465-2024)GE Medical Systems, LLC2024-08-02
Discovery MR450 1.5T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0; Nuc recall (Z-2467-2024)GE Medical Systems, LLC2024-08-02
Optima MR450w 1.5T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0, DV29. recall (Z-2468-2024)GE Medical Systems, LLC2024-08-02
Discovery MR750w 3.0T nuclear magnetic resonance imaging system recall (Z-0135-2022)GE Healthcare, LLC2021-10-16
Discovery MR750 3.0T nuclear magnetic resonance imaging system recall (Z-0136-2022)GE Healthcare, LLC2021-10-16
Optima MR450w 1.5T nuclear magnetic resonance imaging system recall (Z-0140-2022)GE Healthcare, LLC2021-10-16
Discovery MR750w 3.0T - Product Usage: is a whole body magnetic resonance scanner designed recall (Z-2055-2021)GE Healthcare, LLC2021-07-12
Discovery MR750 3.0T - Product Usage: is a whole body magnetic resonance scanner designed recall (Z-2056-2021)GE Healthcare, LLC2021-07-12
Optima MR450w 1.5T, Nuclear Magnetic Resonance Imaging System recall (Z-2063-2021)GE Healthcare, LLC2021-07-12
Discovery MR450 1.5T, Nuclear Magnetic Resonance Imaging System recall (Z-2064-2021)GE Healthcare, LLC2021-07-12
Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and 1.5T Optima MR360 are whole body ma recall (Z-3022-2017)GE Medical Systems, LLC2017-08-02
Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system is a whole body magnetic res recall (Z-3023-2017)GE Medical Systems, LLC2017-08-02
Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system is a whole body magnetic r recall (Z-3024-2017)GE Medical Systems, LLC2017-08-02
Discovery MR750 3.0T Product Usage: Intended use: The Discovery MR750 3.0Tsystem is a whol recall (Z-3025-2017)GE Medical Systems, LLC2017-08-02
Discovery MR450 The systems are whole body magnetic resonance scanners designed to support recall (Z-1188-2017)GE Healthcare, LLC2017-02-10
GE Healthcare, Discovery 3.0T MR750, 5148810-2, 5373011-2, 5499460-2. recall (Z-0201-2019)GE Medical Systems, LLC2015-12-28