Trilogy Evo Universal
K-Number: K181170 · 2019-07-18
ApplicantRespironics, Inc.
Decision Date2019-07-18
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Trilogy Evo Universal is a medical device manufactured by Respironics, Inc.. It received FDA 510(k) clearance on 2019-07-18 under approval number K181170. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Trilogy Evo Universal?
Trilogy Evo Universal is a medical device that received FDA 510(k) clearance on 2019-07-18. It is manufactured by Respironics, Inc.. The 510(k) number is K181170.
When was Trilogy Evo Universal approved by the FDA?
Trilogy Evo Universal received FDA 510(k) clearance on 2019-07-18, under approval number K181170.
What company makes Trilogy Evo Universal?
Trilogy Evo Universal is manufactured by Respironics, Inc..
What is the FDA product code for Trilogy Evo Universal?
The FDA product code for Trilogy Evo Universal is CBK.
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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.