Complement C1q, Antigen, Antiserum, Control

Device Code: 2901

Product Code(s): DAK

Device Classification Information

Device Type ID2901
Device NameComplement C1q, Antigen, Antiserum, Control
Regulation DescriptionComplement Components Immunological Test System.
Regulation Medical SpecialtyImmunology
Review PanelImmunology
Premarket Review Office Of In Vitro Diagnostics And Radiological Health (OIR)
Submission Type510(k)
CFR Regulation Number866.5240 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodeDAK
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 ID2901
DeviceComplement C1q, Antigen, Antiserum, Control
Product CodeDAK
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionComplement Components Immunological Test System.
CFR Regulation Number866.5240 [🔎]
Recalls
Manufacturer Recall Class Date Posted
1
Diagnostic Hybrids, Inc.
III Apr-24-2018
2
Diagnostic Hybrids, Inc.
II Apr-24-2018
TPLC Last Update: 2019-04-02 20:20:53

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