This briefing describes the regulated use of the technology for the indication specified, in the setting described, and with any other specific equipment referred to. It is the responsibility of ...

GE Healthcare announced today the FDA pre-market approval (PMA) for its End-tidal (Et) Control software for general anesthesia delivery on its Aisys CS 2 Anesthesia Delivery System. GE Healthcare is ...

(RTTNews) - GE Healthcare, a healthcare arm of General Electric (GE), said on Monday that it has received pre-market approval from the FDA for its End-tidal Control software to assist in the automated ...

May 13, 2010 — The US Food and Drug Administration (FDA) and General Electric (GE) have issued a class 1 recall of some lots of the GE Aisys and Avance anesthesia systems because of a control board ...

The U.S. Food and Drug Administration has issued a Class I recall of GE Healthcare’s Aisys and Avance Anesthesia systems, due to a defect in control board wiring harnesses, which can cause the machine ...

Please provide your email address to receive an email when new articles are posted on . The U.S. Food and Drug Administration has issued a Class I Medical Device Recall for GE Healthcare’s Aisys and ...

End-tidal Control software helps reduce greenhouse gas emissions and costs by cutting anesthetic agent waste Enables anesthesia providers to set precise targets for oxygen and anesthetic agent Offers ...

In order to maximise sensitivity, the search strategy included 1 concept only: the intervention. Text word and subject heading searches were designed to retrieve records which named the device or the ...