Publication

PS-38: CGA Position Statement on Registration of Facilities Filling Open Topped Medical Liquid Nitrogen Dewars for Device Use in the United States

Abstract

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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Properties

Edition:

Published:

September 2019

Status:

Available To the Public

Size:

1 pages

Publisher:

CGA

Special Attributes:

Notes:

Committee:

Medical Gases

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PS-38: CGA Position Statement on Registration of Facilities Filling Open Topped Medical Liquid Nitrogen Dewars for Device Use in the United States

Abstract

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