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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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EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
EasyDiagnost Eleva DRF (Stitching Patient Support) 706032 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost, Dual-Detector (Stitching Patient Support) 712052 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost Upgrades (Stitching Patient Support) 712083 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
DigitalDiagnost Single Detector (Stitching Patient Support) 712020 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
DigitalDiagnost Release 3 (Stitching Patient Support) 712025 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 Rel.4 Upgrades (Stitching Patient Support) 712084 2 08/17/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
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