Part B: Supplementary Information Sheet (SIS) |
FR Recognition List Number
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052
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Date of Entry 07/15/2019
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FR Recognition Number
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12-326
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Standard | |
NEMA NU 2-2018 Performance Measurements of Positron Emission Tomographs |
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Scope/AbstractThe philosophy and rationale of the standards measurements and illustrative examples of the analysis and results are presented in
Journal of Nuclear Medicine, vol. 43, no. 10, 2002. Daube-Witherspoon ME, Karp JS, Casey ME, DiFilippo FP, Hines H, Muehllehner G, Simcic V, Stearns CW, Adam L-E, Kohlmyer S and Sossi V. "PET Performance Measurements Using the NEMA NU 2-2001 Standard." pp. 1398-1409.
With the exceptions of Section 8 for time-of-flight systems and Section 9 for hybrid PET/CT systems, the Task Force has attempted to specify methods that can be performed on all positron emission tomographs. These include single and multiple slice, discrete and continuous detector, time-of-flight instruments, multi-planar and volume reconstruction models, and dedicated positron emission tomographs as well as other coincidence-capable imaging systems. Wherever possible, future developments that could be readily anticipated were taken into account. |
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Extent of Recognition
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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. |
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Public Law, CFR Citation(s) and Procode(s)*
Regulation Number |
Device Name |
Device Class |
Product Code |
§892.1100 |
Camera, Scintillation (Gamma) |
Class 1 |
IYX |
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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. |
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FDA Technical Contact
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Standards Development Organization
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FDA Specialty Task Group (STG)
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*These are provided as examples and others may be applicable. |