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    • CLIA Currently Waived Analytes

    Metadata Updated: March 16, 2021

    This database contains the commercially marketed in vitro test systems categorized as CLIA waived by the FDA since January 31, 2000, and by the Centers for Disease Control and Prevention (CDC) prior to that date. CLIA waived test systems are waived from certain CLIA laboratory requirements (42 CFR Part 493).

    Access & Use Information

    Public: This dataset is intended for public access and use. License: See this page for license information.

    Downloads & Resources

    Dates

    Metadata Created Date November 10, 2020
    Metadata Updated Date March 16, 2021

    Metadata Source

    Harvested from Healthdata.gov

    Other Data Resources

    Additional Metadata

    Resource Type Dataset
    Metadata Created Date November 10, 2020
    Metadata Updated Date March 16, 2021
    Publisher U.S. Food and Drug Administration
    Maintainer
    Identifier 3f3f0bb7-1c03-415a-90ca-400bfc08f096
    Data First Published 2021-02-25
    Data Last Modified 2013-11-01
    Public Access Level public
    Bureau Code 009:10
    Metadata Context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
    Metadata Catalog ID https://healthdata.gov/data.json
    Schema Version https://project-open-data.cio.gov/v1.1/schema
    Catalog Describedby https://project-open-data.cio.gov/v1.1/schema/catalog.json
    Harvest Object Id c71d3131-bc2c-4e5d-a261-2b02705bbdb1
    Harvest Source Id 651e43b2-321c-4e4c-b86a-835cfc342cb0
    Harvest Source Title Healthdata.gov
    Homepage URL http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfClia/analyteswaived.cfm
    License http://opendefinition.org/licenses/odc-odbl/
    Program Code 009:005
    Source Datajson Identifier True
    Source Hash 02cba87dd741173907a0b807baeef121cbb5316c
    Source Schema Version 1.1

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