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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 28 Results
510(K) Number: K090625
 
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Product Description
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DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost Release 3 (Stitching Patient Support) 712025 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
BuckyDiagnost Ceiling System (Stitching Patient Support) 704031 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
CombiDiagnost R90 (Stitching Patient Support) 709030 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
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