510(k) K240303

Device
MetaLite DX Digital Pathology Software
Applicant
Jellox Biotech, Inc.
510(k) number
K240303
Product code
QKQ
Decision
Substantially Equivalent (SESE)
Decision date
2024-10-28
Date received
2024-02-02
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
Fan Tzu-Han
Address
# 66-5, Shengyi 5th Rd., Zhubei City Hsinchu County TW 302041 302041

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
K243449INFINITT DPSInfinitt Healthcare Co., Ltd.2025-12-09
K252762HALO AP DxIndica Labs, LLC2025-11-25
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
K233126aetherSlideAetherai Co., Ltd.2024-05-30
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