FDA 510(k), K173626, Celerity 20 Steam Process Challenge Device for Dynamic Air Removal Cycles

FDA 510(k), K173626, Celerity 20 Steam Process Challenge Device for Dynamic Air Removal Cycles

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510(K) Number: K173626
Device Name: Celerity 20 Steam Process Challenge Device for Dynamic Air Removal Cycles
Manufacturer: STERIS Corporation
Device Classification Name: indicator, biological sterilization process
Regulation Number: 880.2800
Classification Product Code: FRC
Date Received: 11/24/2017
Decision Date: 02/21/2018
Regulation Medical Specialty: General Hospital

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