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FDA approves Fujirebio's Lumipulse G B•R•A•H•M•S PCT assay

01:38 EDT 13 Jun 2018 | Medical Business Review

Fujirebio Diagnostics, a consolidated subsidiary of Miraca Holdings, has secured approval from the US Food and Drug Administration (FDA) for its Lumipulse G B•R•A•H•M•S procalcitonin (PCT) assay to be tested on Lumipulse G1200 immunoassay platform.

Original Article: FDA approves Fujirebio's Lumipulse G B•R•A•H•M•S PCT assay

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