Admira Fusion 5
K-Number: K230877 · 2023-07-13
ApplicantVoco GmbH
Decision Date2023-07-13
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Admira Fusion 5 is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2023-07-13 under approval number K230877. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Admira Fusion 5?
Admira Fusion 5 is a medical device that received FDA 510(k) clearance on 2023-07-13. It is manufactured by Voco GmbH. The 510(k) number is K230877.
When was Admira Fusion 5 approved by the FDA?
Admira Fusion 5 received FDA 510(k) clearance on 2023-07-13, under approval number K230877.
What company makes Admira Fusion 5?
Admira Fusion 5 is manufactured by Voco GmbH.
What is the FDA product code for Admira Fusion 5?
The FDA product code for Admira Fusion 5 is EBF.
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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.