CELERITY 20 Steam Process Challenge Device for Gravity Cycles
K-Number: K173629 · 2018-02-21
ApplicantSTERIS Corporation
Decision Date2018-02-21
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
CELERITY 20 Steam Process Challenge Device for Gravity Cycles is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2018-02-21 under approval number K173629. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CELERITY 20 Steam Process Challenge Device for Gravity Cycles?
CELERITY 20 Steam Process Challenge Device for Gravity Cycles is a medical device that received FDA 510(k) clearance on 2018-02-21. It is manufactured by STERIS Corporation. The 510(k) number is K173629.
When was CELERITY 20 Steam Process Challenge Device for Gravity Cycles approved by the FDA?
CELERITY 20 Steam Process Challenge Device for Gravity Cycles received FDA 510(k) clearance on 2018-02-21, under approval number K173629.
What company makes CELERITY 20 Steam Process Challenge Device for Gravity Cycles?
CELERITY 20 Steam Process Challenge Device for Gravity Cycles is manufactured by STERIS Corporation.
What is the FDA product code for CELERITY 20 Steam Process Challenge Device for Gravity Cycles?
The FDA product code for CELERITY 20 Steam Process Challenge Device for Gravity Cycles is FRC.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.