510(k) K233126

Device
aetherSlide
Applicant
Aetherai Co., Ltd.
510(k) number
K233126
Product code
QKQ
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-30
Date received
2023-09-27
Regulation
864.3700
Classification name
Digital Pathology Image Viewing And Management Software
Medical specialty
Pathology
Review panel
Pathology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Leticia Hong
Address
15f & 15f-1., # 508, Sec. 7 Zhongxiao E. Rd., Nangang Dist. Taipei City TW 115011 115011

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QKQ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K243391AISight DxPathAI, Inc.2025-06-26
K250968PathPresenter Clinical ViewerPathpresenter Corporation2025-06-20
K250414CaloPixTribun Health2025-05-14
K242244Viewer+Lumea, Inc.2025-03-14
K241273FullFocusPaige.Ai, Inc.2025-01-09
K240303MetaLite DX Digital Pathology SoftwareJellox Biotech, Inc.2024-10-28
K212361NovoPathAI, Inc.2022-08-11
K210811Dynamyx Digital Pathology SoftwareInspirata, Inc.2022-03-01
K201005FullFocusPaige.Ai, Inc.2020-07-15
K193054Sectra Digital Pathology ModuleSectra AB2020-03-31