SQ.line KERRISON
K-Number: K223596 · 2023-06-29
ApplicantAesculap, Inc.
Decision Date2023-06-29
Product CodeHAE
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
SQ.line KERRISON is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2023-06-29 under approval number K223596. The device is classified under product code HAE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SQ.line KERRISON?
SQ.line KERRISON is a medical device that received FDA 510(k) clearance on 2023-06-29. It is manufactured by Aesculap, Inc.. The 510(k) number is K223596.
When was SQ.line KERRISON approved by the FDA?
SQ.line KERRISON received FDA 510(k) clearance on 2023-06-29, under approval number K223596.
What company makes SQ.line KERRISON?
SQ.line KERRISON is manufactured by Aesculap, Inc..
What is the FDA product code for SQ.line KERRISON?
The FDA product code for SQ.line KERRISON is HAE.
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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.