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

Clearance record K183294

CELERITY 20 HP Biological Indicator, CELERITY HP Challenge Pack · STERIS Corporation · decided 2019-01-03 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
CelerityLCB044STERIS CORPORATIONFRC10724995154230
CelerityLCB045STERIS CORPORATIONFRC10724995161597