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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 052 Date of Entry 07/15/2019 
FR Recognition Number 12-326
Standard
NEMA NU 2-2018
Performance Measurements of Positron Emission Tomographs
Scope/Abstract
The 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.
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.
Public Law, CFR Citation(s) and Procode(s)*
Regulation Number Device Name Device Class Product Code
§892.1100 Camera, Scintillation (Gamma) Class 1 IYX
FDA Technical Contact
 S. Andrew Kang
  FDA/OC/CDRH/OPEQ/OIDRH/DRH/NMRTB/
  301-796-6544
  s.kang@fda.hhs.gov
Standards Development Organization
NEMA National Electrical Manufacturers Association https://www.nema.org/
FDA Specialty Task Group (STG)
Radiology
*These are provided as examples and others may be applicable.
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