CHIKAI Nexus petit
K-Number: K252011 · 2026-02-02
ApplicantAsahi Intecc Co., Ltd.
Decision Date2026-02-02
Product CodeMOF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
CHIKAI Nexus petit is a medical device manufactured by Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2026-02-02 under approval number K252011. The device is classified under product code MOF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CHIKAI Nexus petit?
CHIKAI Nexus petit is a medical device that received FDA 510(k) clearance on 2026-02-02. It is manufactured by Asahi Intecc Co., Ltd.. The 510(k) number is K252011.
When was CHIKAI Nexus petit approved by the FDA?
CHIKAI Nexus petit received FDA 510(k) clearance on 2026-02-02, under approval number K252011.
What company makes CHIKAI Nexus petit?
CHIKAI Nexus petit is manufactured by Asahi Intecc Co., Ltd..
What is the FDA product code for CHIKAI Nexus petit?
The FDA product code for CHIKAI Nexus petit is MOF.
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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.