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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K052078
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Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Intera 1.0T Power/Pulsar, Model Number 781103. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Num... 2 03/20/2015 FEI # 1218950
Philips Medical Systems, Inc.
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