510(k) K251883

Device
MIM – LesionID Pro
Applicant
Mim Software, Inc.
510(k) number
K251883
Product code
LLZ
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-11
Date received
2025-06-20
Regulation
892.2050
Classification name
System, Image Processing, Radiological
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Sydney Lindner
Address
25800 Science Park Dr., Suite 180 Cleveland OH US 44122 44122

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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