← FDA Medical Device Classifications

Covid-19 Test Home Collection Kit Devices

QLW · Not classified · Unknown

Classification

FDA Product Code
QLW
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

Specimens collected using the Home Collection Kit can be transported at ambient temperature for testing at a laboratory. SARS-CoV-2 RNA from the clinical specimen is maintained in the specimen packaging and suitable for use in diagnostic testing preformed using a molecular in vitro diagnostic (IVD) test for the detection of SARS-CoV-2 RNA that is authorized for use with the COVID-19 Test Home Collection Kit.

Market data

Cleared 510(k) submissions
0
Registered establishments
4

Source

Authoritative
FDA Device Classification database
Machine
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