510(k) K230899

Device
qXR-PTX-PE
Applicant
Qure.Ai Technologies
510(k) number
K230899
Product code
QFM
Decision
Substantially Equivalent (SESE)
Decision date
2023-08-22
Date received
2023-03-31
Regulation
892.2080
Classification name
Radiological Computer-Assisted Prioritization Software For Lesions
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Ayushi Mahendra
Address
Level 7, Commerz Ii International Business Park Oberoi Garden City, Goregaon (E) Mumbai IN 400 063 400 063

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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