Celerity Incubator
K-Number: K213881 · 2022-07-21
ApplicantSTERIS Corporation
Decision Date2022-07-21
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Celerity Incubator is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2022-07-21 under approval number K213881. 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 Incubator?
Celerity Incubator is a medical device that received FDA 510(k) clearance on 2022-07-21. It is manufactured by STERIS Corporation. The 510(k) number is K213881.
When was Celerity Incubator approved by the FDA?
Celerity Incubator received FDA 510(k) clearance on 2022-07-21, under approval number K213881.
What company makes Celerity Incubator?
Celerity Incubator is manufactured by STERIS Corporation.
What is the FDA product code for Celerity Incubator?
The FDA product code for Celerity Incubator 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.