FDA Device Intelligence
HomeDevice types › QLW

Covid-19 Test Home Collection Kit Devices

FDA product code QLW · Class N · Unknown

2
Registered devices
4
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-01-24Matrix Medical NetworkDue to COVID-19 Test not being authorized for home sample collection.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.