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U.S. Department of Health and Human Services

Recognized Consensus Standards

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Part B: Supplementary Information Sheet (SIS)
FR Recognition List Number 056 Date of Entry 06/07/2021 
FR Recognition Number 8-556
ASTM F640-20
Standard Test Methods for Determining Radiopacity for Medical Use
1.1 These test methods cover the determination of the radiopacity of materials and products utilizing X-ray based techniques, including fluoroscopy, angiography, CT (computed tomography), and DEXA (dual energy X-ray absorptiometry), also known as DXA, The results of these measurements are an indication of the likelihood of locating the product within the human body.

1.2 Radiopacity is determined by (a) qualitatively comparing image(s) of a test specimen and a user-defined standard, with or without the use of a body mimic; or (b) quantitatively determining the specific difference in optical density or pixel intensity between the image of a test specimen and the image of a user-defined standard, with or without the use of a body mimic.
Extent of Recognition
Complete standard
Rationale for Recognition
This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies.
Transition Period
FDA recognition of ASTM F640-12 [Rec# 8-418] will be superseded by recognition of ASTM F640-20 [Rec# 8-556]. FDA will accept declarations of conformity, in support of premarket submissions, to [Rec# 8-418] until July 10, 2022. After this transition period, declarations of conformity to [Rec# 8-418] will not be accepted.
FDA Technical Contact
 Terry O. Woods
Standards Development Organization
ASTM ASTM International http://www.astm.org/
FDA Specialty Task Group (STG)