Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

aetherSlide

K-Number: K233126 · 2024-05-30

ApplicantAetherai Co., Ltd.
Decision Date2024-05-30
Product CodeQKQ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

aetherSlide is a medical device manufactured by Aetherai Co., Ltd.. It received FDA 510(k) clearance on 2024-05-30 under approval 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. It is manufactured by Aetherai Co., Ltd.. The 510(k) number is K233126.

When was aetherSlide approved by the FDA?

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

What company makes aetherSlide?

aetherSlide is manufactured by Aetherai Co., Ltd..

What is the FDA product code for aetherSlide?

The FDA product code for aetherSlide is QKQ.

Related Devices (Code: QKQ)

K201005FullFocusPaige.Ai, Inc. K193054Sectra Digital Pathology ModuleSectra AB K212361NovoPathAI, Inc. K210811Dynamyx Digital Pathology SoftwareInspirata, Inc. K240303MetaLite DX Digital Pathology SoftwareJellox Biotech, Inc. K243449INFINITT DPSInfinitt Healthcare Co., Ltd.

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.

↑