Teleflex Receives FDA 510(k) Clearance for Anesthetic Gas-Blocking Mask

Limerick, Pa.-based Teleflex received FDA 510(k) clearance for its ISO-Gard Mask with CleanAir Technology, designed to reduce harmful anesthetic gases clinicians are exposed to.

Patients recovering from surgery in the post-anesthesia care unit exhale gases and nurses, upon ingesting the byproduct, can experience side effects including nausea, dizziness, headaches and fatigue, according to the report.

Teleflex's CleanAir technology forces a unidirectional flow of oxygen through the mask to reduce waste gas leakage and improve patient delivery.

More Articles on Anesthesia:
ASA Lauds CMS for Proposal to Mandate Physician Supervision of Nurse Anesthetists
Study: Isoflurane Exposure Led to Apoptotic Cell Death in Mice
Chicago-Area Anesthesia Practices Merge, Open Midwest Anesthesia Partners


Copyright © 2024 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.

 

Featured Whitepapers

Featured Webinars