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U.S. Department of Health and Human Services

Recognized Consensus Standards: Medical Devices
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Part B: Supplementary Information Sheet (SIS)
FR Recognition List Number 062 Date of Entry 05/29/2024 
FR Recognition Number 12-361
Standard
ICDM  IDMS Version 1.2 May 2023
Information Display Measurements Standard
Scope/Abstract
The IDMS specifies standard measurement procedures, test patterns, measurement report templates, and testing software to quantify electronic display characteristics and qualities. The document is applicable to various types of displays including non-see-through (virtual reality) and see-through type (augmented reality) eyewear displays.
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.
Relevant FDA Guidance and/or Supportive Publications*
Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices - Guidance for Industry and Food and Drug Administration Staff, issued September 2018.
FDA Technical Contacts
 Ryan Beams
  FDA/OC/CDRH/OSEL/DIDSR/
  240-402-3216
  ryan.beams@fda.hhs.gov
 Chumin Zhao
  FDA/OC/CDRH/OSEL/DIDSR/
  --
  chumin.zhao@fda.hhs.gov
Standards Development Organization
ICDM International Committee for Display Metrology https://www.sid.org/Standards/ICDM#8271481-contact
FDA Specialty Task Group (STG)
Radiology
*These are provided as examples and others may be applicable.
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