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

Clearance record K232500

Lumify Diagnostic Ultrasound System · Philips Ultrasound · decided 2023-10-26 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Lumify Diagnostic Ultrasound System795005Philips Ultrasound LLCITX IYN IYO QIH00884838122116