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U.S. Department of Health and Human Services

Product Classification

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Device radioimmunoassay, tricyclic antidepressant drugs
Regulation Description Tricyclic antidepressant drugs test system.
Regulation Medical Specialty Toxicology
Review Panel Toxicology
Product CodeLFG
Submission Type 510(k)
Regulation Number 862.3910
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Third Party Review
Accredited Persons

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