Aesculap AICON Container
K-Number: K214041 · 2022-12-30
ApplicantAesculap, Inc.
Decision Date2022-12-30
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Aesculap AICON Container is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2022-12-30 under approval number K214041. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Aesculap AICON Container?
Aesculap AICON Container is a medical device that received FDA 510(k) clearance on 2022-12-30. It is manufactured by Aesculap, Inc.. The 510(k) number is K214041.
When was Aesculap AICON Container approved by the FDA?
Aesculap AICON Container received FDA 510(k) clearance on 2022-12-30, under approval number K214041.
What company makes Aesculap AICON Container?
Aesculap AICON Container is manufactured by Aesculap, Inc..
What is the FDA product code for Aesculap AICON Container?
The FDA product code for Aesculap AICON Container is KCT.
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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.