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U.S. Department of Health and Human Services

Product Classification
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Device uranyl acetate/zinc acetate, sodium
Regulation Description Sodium test system.
Regulation Medical Specialty Clinical Chemistry
Review Panel Clinical Chemistry
Product CodeCEI
Submission Type 510(k)
Regulation Number 862.1665
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Guidance Document
  • Guidance for Industry In Vitro Diagnostic Sodium Test System; Final [http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm093923.htm] 
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