Immunoelectrophoretic, Immunoglobulins, (g, A, M)

Device Code: 2872

Product Code(s): CFF

Device Classification Information

Device Type ID2872
Device NameImmunoelectrophoretic, Immunoglobulins, (g, A, M)
Regulation DescriptionImmunoglobulins A, G, M, D, And E Immunological Test System.
Regulation Medical SpecialtyImmunology
Review PanelImmunology
Premarket Review Office Of In Vitro Diagnostics And Radiological Health (OIR)
Submission Type510(k)
CFR Regulation Number866.5510 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodeCFF
GMP ExemptNo
Summary MREligible
Implanted DeviceNo
Life Support DeviceNo
Third Party Review Eligible For Accredited Persons Expansion Pilot Program

Recognized Standards

Total Product Life Cycle

Device Type ID2872
DeviceImmunoelectrophoretic, Immunoglobulins, (g, A, M)
Product CodeCFF
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionImmunoglobulins A, G, M, D, And E Immunological Test System.
CFR Regulation Number866.5510 [🔎]
Premarket Reviews
ManufacturerDecision
SEBIA
 
SUBSTANTIALLY EQUIVALENT
3
TPLC Last Update: 2019-04-02 20:20:23

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