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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 17 Results
510(K) Number: K162931
 
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Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic d... 2 09/03/2021 FEI # 3016618143
Philips North America Llc
Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagn... 2 09/03/2021 FEI # 3016618143
Philips North America Llc
SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for ... 2 09/03/2021 FEI # 3016618143
Philips North America Llc
Conversion SmarthPath to dStream for 1.5T, Model 781260 Product Usage: Indicated for use as a di... 2 04/18/2018 FEI # 1218950
Philips Electronics North America Corporation
Ingenia 1.5T CX (ZBO), Model Number 781262. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Ingenia 1.5T CX, Models 781261 & 781262 Product Usage: Indicated for use as a diagnostic device.... 2 04/18/2018 FEI # 1218950
Philips Electronics North America Corporation
Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems indicated for use as a diagnost... 2 08/25/2021 FEI # 3016618143
Philips North America Llc
Ingenia 3.0T CX, Model Number 781271. Nuclear Magnetic Resonance Imaging System 2 02/22/2019 FEI # 3002807880
Philips Medical Systems Nederlands
Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic de... 2 09/03/2021 FEI # 3016618143
Philips North America Llc
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