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FDA 510(k)

LARS ACJ

K-Number: K253115 · 2026-06-10

Decision Date2026-06-10
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LARS ACJ is the device name listed in this FDA 510(k) record. The listed applicant is Movmedix S.A.S.. It received FDA 510(k) clearance on 2026-06-10 under 510(k) number K253115. The device is classified under product code HTN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARS ACJ?

LARS ACJ is a medical device that received FDA 510(k) clearance on 2026-06-10. The listed applicant is Movmedix S.A.S.. The 510(k) number is K253115.

When did LARS ACJ receive FDA 510(k) clearance?

LARS ACJ received FDA 510(k) clearance on 2026-06-10, under 510(k) number K253115.

Who is the listed applicant for LARS ACJ?

The FDA 510(k) record lists Movmedix S.A.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LARS ACJ?

The FDA product code for LARS ACJ is HTN.

Related Devices (Code: HTN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.