aetherSlide— 510(k) K233126

Substantially Equivalent

Aetherai Co., Ltd.

FDA 510(k) clearance K233126 for aetherSlide, Substantially Equivalent on 2024-05-30. Applicant: Aetherai Co., Ltd.. Device class: 2.

Clearance details

Applicant: Aetherai Co., Ltd.
Product code: Code QKQ
Device class: Class 2
Regulation: 21 CFR 864.3700
Advisory panel: Pathology
Date received: 2023-09-27
Decision date: 2024-05-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei City, TW

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.