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U.S. Department of Health and Human Services

Product Classification
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Device lead, atomic absorption
Regulation Description Lead test system.
Regulation Medical Specialty Toxicology
Review Panel Toxicology
Product CodeDOF
Premarket Review Office of In Vitro Diagnostics (OHT7)
Division of Chemistry and Toxicology Devices (DCTD)
Submission Type 510(k)
Regulation Number 862.3550
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting		 Ineligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible
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