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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 11 Results
510(K) Number: K030520
 
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Intera 1.5T Power/Pulsar, Model Number 781105. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 Philips Medical Systems Nederlands
Intera 3.0T Master/Quasar Dual, Model Number 781150. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 Philips Medical Systems Nederlands
Intera 1.5T Explorer/Nova Dual, Model Number 781108. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 Philips Medical Systems Nederlands
Intera 0.5T Standard, Model Number 781101. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 Philips Medical Systems Nederlands
Intera 1.5T Omni/Stellar, Model Number 781104. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 Philips Medical Systems Nederlands
Intera 1.5T R11, Model Number 781170. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 Philips Medical Systems Nederlands
Intera 1.5T Master/Nova, Model Number 781106. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 Philips Medical Systems Nederlands
Intera 1.5T CV, Model Number 781107. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 Philips Medical Systems Nederlands
Intera 1.0T; 1) Stellar Model 781102, 2) Pular Model 781103 Product Usage: Indicated for use as... 2 04/18/2018 Philips Electronics North America Corporation
Intera 0.5T Standard, Model 781101 Product Usage: Indicated for use as a diagnostic device. It c... 2 04/18/2018 Philips Electronics North America Corporation
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