Part B: Supplementary Information Sheet (SIS) |
FR Recognition List Number
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020
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Date of Entry 09/09/2008
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FR Recognition Number
|
13-24
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Standard | |
CLSI LIS09-A Standard Guide for Coordination of Clinical Laboratory Services within the Electronic Health Record Environment and Networked Architectures |
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Scope/AbstractThis guide covers the process of defining and documenting the capabilities, sources, and pathways of data exchange within a given network architecture of a Health Information Network (HIN) serving a set of constituents. |
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Extent of Recognition
|
Public Law, CFR Citation(s) and Procode(s)*
Regulation Number |
Device Name |
Device Class |
Product Code |
§862.2100 |
Calculator/Data Processing Module, For Clinical Use |
Class 1 |
JQP |
|
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
|
Standards Development Organization
|
FDA Specialty Task Group (STG)
|
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*These are provided as examples and others may be applicable. |