510(k) K241273

Device
FullFocus
Applicant
Paige.Ai, Inc.
510(k) number
K241273
Product code
QKQ
Decision
Substantially Equivalent (SESE)
Decision date
2025-01-09
Date received
2024-05-06
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
Mufaddal Jafferji
Address
11 Times Sq. Floor 37 New York NY US 10036 10036

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
K240303MetaLite DX Digital Pathology SoftwareJellox Biotech, Inc.2024-10-28
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