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U.S. Department of Health and Human Services

Product Classification

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Device acid, phosphoric-tungstic (spectrophotometric), chloride
Regulation Description Chloride test system.
Regulation Medical Specialty Clinical Chemistry
Review Panel Clinical Chemistry
Product CodeCHG
Premarket Review Office of In Vitro Diagnostics and Radiological Health (OIR)
Submission Type 510(k)
Regulation Number 862.1170
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Guidance Document
  • Guidance for Industry In Vitro Diagnostic Chloride Test System; Final [http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm093851.htm] 
Third Party Review
Accredited Persons

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