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CGA PS-38

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

Position Statement by Compressed Gas Association , 09/24/2019

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About This Item

 

Full Description

This publication provides CGA's 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.

 

Product Details

Edition:
2nd
Published:
09/24/2019
Number of Pages:
2
File Size:
1 file , 130 KB
Note:
This product is unavailable in Russia, Ukraine, Belarus
 

Document History

  1. CGA PS-38

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    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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  2. CGA PS-38


    CGA Position Statement on Registration of Facilities Filling Open Topped Medical Nitrogen Dewars for Device Use

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