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U.S. Department of Health and Human Services

Product Classification

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Device antigen, latex agglutination, entamoeba histolytica & rel. spp.
Regulation Description Entamoeba histolyticaserological reagents.
Regulation Medical Specialty Microbiology
Review Panel Microbiology
Product CodeGMO
Premarket Review Office of In Vitro Diagnostics and Radiological Health (OIR)
Submission Type 510(K) Exempt
Regulation Number 866.3220
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
    Note: Class II devices the Food and Drug Administration (FDA) has also published a list of Class II (special controls) devices subject to certain limitations, that are now exempt from the premarket notification requirements under the Food and Drug Administration Modernization Act of 1997 (the Modernization Act). FDA believes that these exemptions will relieve manufacturers from the need to submit premarket notification submissions for these devices and will enable FDA to redirect the resources that would be spent on reviewing such submissions to more significant public health issues. FDA is taking this action in order to meet a requirement of the Modernization Act.
Recognized Consensus Standard
Third Party Review Not Third Party Eligible
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