Immunofluorescent Assay, T. Cruzi

Device Code: 3487

Product Code(s): MIV

Device Classification Information

Device Type ID3487
Device NameImmunofluorescent Assay, T. Cruzi
Regulation DescriptionTrypanosoma Spp. Serological Reagents.
Regulation Medical SpecialtyMicrobiology
Review PanelMicrobiology
Premarket Review Office Of In Vitro Diagnostics And Radiological Health (OIR)
Submission Type510(k)
CFR Regulation Number866.3870 [🔎]
FDA Device ClassificationClass 1 Medical Device
Product CodeMIV
GMP ExemptNo
Summary MREligible
Implanted DeviceNo
Life Support DeviceNo
Third Party Review Eligible For Accredited Persons Program

Recognized Standards

Total Product Life Cycle

Device Type ID3487
DeviceImmunofluorescent Assay, T. Cruzi
Product CodeMIV
FDA Device ClassificationClass 1 Medical Device
Regulation DescriptionTrypanosoma Spp. Serological Reagents.
CFR Regulation Number866.3870 [🔎]
TPLC Last Update: 2019-04-02 20:31:00

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