June 12, 2007 -- The US Food and Drug Administration (FDA) has granted 510(k) clearances for an intermittent pneumatic compression device for the treatment of chronic venous insufficiency, venous ...
Jan Davidson, RN, MSN, is the new AORN perioperative education specialist who has a focus on ambulatory surgery centers. Q: I am trying to determine what the best practice is relative to applying IPC ...
LOS ALTOS HILLS, Calif.--(BUSINESS WIRE)--Fist Assist Devices, LLC, announces completion of the non-significant risk FACT Trial (Fist Assist Clinical Trial). FACT evaluated the use of an intermittent ...
LOS ALTOS HILLS, Calif.--(BUSINESS WIRE)--Fist Assist Devices, LLC, announces that data associated with the p-FACT cohort, a data subset of the recently completed, non-significant risk Fist Assist ...
According to a patient safety toolkit, released by AAAHC’s Institute for Quality Improvement, some procedures commonly performed in the ambulatory surgery center setting have relatively high risks for ...
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