510(k) K261595

Device
Ceevra Reveal 4
Applicant
Ceevra, Inc.
510(k) number
K261595
Product code
QIH
Decision
Substantially Equivalent (SESE)
Decision date
2026-08-25
Date received
2026-05-14
Regulation
892.2050
Classification name
Automated Radiological Image Processing Software
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Ken Koster
Address
465 California St. 7th Floor San Francisco CA US 94104 94104

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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