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Covid-19 Multi-Analyte Antigen Device

QMN · Not classified · Unknown

Classification

FDA Product Code
QMN
Device class
Not classified
Regulation
Review panel
MI
Medical specialty
Unknown
Submission type
8
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

Definition

A COVID-19 Multi-Analyte Antigen Device is a test for the qualitative detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and common respiratory microorganisms in human respiratory and/or acceptable clinical specimens collected from individuals suspected of respiratory viral infection consistent with COVID-19 by a healthcare provider. Results should not be interpreted in the context of clinical observations, patient history, and/or epidemiological information, patient history, and/or epidemiological information.

Market data

Cleared 510(k) submissions
0
Registered establishments
26

Source

Authoritative
FDA Device Classification database
Machine
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