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

Clearance record K233065

V-PRO maX 2 Low Temperature Sterilization System · Steris · decided 2023-10-20 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
VAPROXPB007STERIS CORPORATIONMLR00724995089160
VAPROXPB011STERIS CORPORATIONMLR00724995153090
VAPROXPB012STERIS CORPORATIONMLR00724995153106
VAPROXPB028STERIS CORPORATIONMLR00724995089511