FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Image Suite

K Number: K251168 · Decision Sep 4, 2025
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
48
Review Days
142

Basic Information

Device Name
Image Suite
K Number
K251168
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carestream Health, Inc.
Date Received
April 15, 2025
Decision Date
September 4, 2025
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

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