CGA PS-38 2nd Edition

Current Revision
CGA Position Statement on Registration of Facilities Filling Open Topped Medical Liquid Nitrogen Dewars for Device Use in the United States

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CGA PS-38 2nd Edition
Provides CGA position on procedures that a filler of open topped medical liquid nitrogen dewars should follow and whether they need to register with the U.S. Food and Drug Administration (FDA) as a device manufacturing facility.
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