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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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.
Related Articles on Anesthesia:
ASA Presents 6 Tactics to Relieve Drug Shortages
Cleveland Clinic Anesthesiologist Resuscitates Newborn While on Duty as Cop
Study: Patient Expectations Alter the Effect of Analgesia