FDA 510(k)

aetherSlide

K-Number: K233126 · 2024-05-30

Decision Date2024-05-30

Product CodeQKQ

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

aetherSlide is the device name listed in this FDA 510(k) record. The listed applicant is Aetherai Co., Ltd.. It received FDA 510(k) clearance on 2024-05-30 under 510(k) number K233126. The device is classified under product code QKQ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the aetherSlide?

aetherSlide is a medical device that received FDA 510(k) clearance on 2024-05-30. The listed applicant is Aetherai Co., Ltd.. The 510(k) number is K233126.

When did aetherSlide receive FDA 510(k) clearance?

aetherSlide received FDA 510(k) clearance on 2024-05-30, under 510(k) number K233126.

Who is the listed applicant for aetherSlide?

The FDA 510(k) record lists Aetherai Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for aetherSlide?

The FDA product code for aetherSlide is QKQ.

Related Devices (Code: QKQ)

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.

K253561Aperio iQC DX SoftwareLeica Biosystems Imaging, Inc.K261380Concentriq AP-DxProscia, Inc.K243449INFINITT DPSInfinitt Healthcare Co., Ltd.K252762HALO AP DxIndica Labs, LLC K243391AISight DxPathAI, Inc.K250968PathPresenter Clinical ViewerPathpresenter Corporation

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.