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U.S. Department of Health and Human Services

Product Classification

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Device guaiac reagent
Regulation Description Occult blood test.
Regulation Medical Specialty Hematology
Review Panel Hematology
Product CodeGGG
Premarket Review Office of In Vitro Diagnostics (OHT7)
Division of Immunology and Hematology Devices (DIHD)
Submission Type 510(k)
Regulation Number 864.6550
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Eligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review
Accredited Persons
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