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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K935047
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Program Update Package AutoDELFIA® 3.0, Fluorometer, for clinical use Product Number: 1235-8110 ... 3 10/11/2018 FEI # 3006159931
PerkinElmer Health Sciences, Inc.
DELFIA® PC with V3.0 Software, Fluorometer, for clinical use Product Number: 1235-8100 Product ... 3 10/11/2018 FEI # 3006159931
PerkinElmer Health Sciences, Inc.
AutoDELFIA® Plate Processor , Fluorometer, for clinical use Product Number: 1235-5110 Product... 3 10/11/2018 FEI # 3006159931
PerkinElmer Health Sciences, Inc.
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