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U.S. Department of Health and Human Services

Product Classification

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Device system, x-ray, tomographic
Regulation Description Tomographic x-ray system.
Regulation Medical Specialty Radiology
Review Panel Radiology
Product CodeIZF
Premarket Review Office of In Vitro Diagnostics and Radiological Health (OIR)
Submission Type 510(k)
Regulation Number 892.1740
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Third Party Review
Accredited Persons

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