Maquet Flow-i Anesthesia System Receives FDA Approval

The Food and Drug Administration has approved Maquet's FLOW-i anesthesia system for 510(k) marketing, according to a MedGadget report.

The anesthesia machine features advanced monitoring and respiratory controls as well as a re-breathing device that allows partial re-circulation of exhaled gases.

The approval applies to C20, C30 and C40 models of the system, according to the company.

Read the MedGadget report on the FLOW-i anesthesia system.

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