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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K222205

Cold Sore Device (Model: QPZ-01) · Light Tree Ventures Europe B.V. · decided 2022-10-07 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Walgreens845575WALGREEN CO.OKJ00311917065007
WALGREENSQPZ-01WALGREEN CO.OKJ00311917130347