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U.S. Department of Health and Human Services

Recognized Consensus Standards

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Recognition List Number: 031 FR Publication Date: 08/05/2013 

Part B: Supplementary Information

Recognition Number 13-37: CLSI AUTO7-A, laboratory automation: data content for specimen identification; approved standard. (Software/Informatics)

Date of Standard: 2004. 
Address of Standards Development Organization:
 Clinical Laboratory Standards Institute (CLSI)
  950 West Valley Road
  Suite 2500
  Wayne, PA 19087
 
CDRH Office and Division associated with recognized standards:
OFFICE OF IN VITRO DIAGNOSTICS AND RADIOLOGICAL HEALTH (OIR)
Devices Affected:
Lab Information Systems, Auto Analysis
Processes Affected:
510(k), PMA, PDP
Type of Standard:
 Vertical, National
Extent of Recognition:
Complete standard
Related CFR Citations and Product Codes:
Regulation
Number
Device Name Device
Class
Product
Code
§862.2100 Calculator/Data Processing Module, For Clinical Use Class 1 JQP
FDA Technical Contact:
 James Callaghan
  FDA/CDRH/OIR
  10903 New Hampshire Avenue Building 66, Room 5658
  Silver Spring MD 20993
  301/796-6137
  email: james.callaghan@fda.hhs.gov
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