Publication
PS-38: CGA Position Statement on Registration of Facilities Filling Open Topped Medical Liquid Nitrogen Dewars for Device Use in the United States
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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Edition:
2
Published:
September 2019
Status:
Available To the Public
Size:
1 pages
Publisher:
CGA
Special Attributes:
Notes:
Committee:
Medical Gases
Keywords
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