Last synced on 20 December 2024 at 11:05 pm

Reagent, Coronavirus Serological

Page Type
Product Code
Definition
The qualitative detection of IgM and/or IgG antibodies to coronavirus from human specimens.
Physical State
In vitro diagnostic device.
Technical Method
Serological assay.
Target Area
Detection and differentiation of IgM and/or IgG antibodies from human specimens.
Review Panel
Microbiology
Submission Type
EUA - Emergency Use Authorization
Device Classification
N
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

As product code QKO is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.

Reagent, Coronavirus Serological

Page Type
Product Code
Definition
The qualitative detection of IgM and/or IgG antibodies to coronavirus from human specimens.
Physical State
In vitro diagnostic device.
Technical Method
Serological assay.
Target Area
Detection and differentiation of IgM and/or IgG antibodies from human specimens.
Review Panel
Microbiology
Submission Type
EUA - Emergency Use Authorization
Device Classification
N
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

As product code QKO is assigned to devices that are "not-classified", it is not linked to any specific regulation and CFR section.