Cleared Traditional

KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI (K923270) - FDA 510(k) Clearance

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K923270 · Eastman Kodak Company · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1992
Decision
67d
Days
Class 2
Risk

K923270 is an FDA 510(k) clearance for the KODAK EKTASCAN IMAGELINK QUALITY CONTROL WORKSTATI. Classified as System, Image Processing, Radiological within the LLZ classification (a category encompassing advanced image processing and PACS-adjacent software), Class II - Special Controls.

Submitted by Eastman Kodak Company (Rochester, US). The FDA issued a Cleared decision on September 11, 1992 after a review of 67 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2050 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Incremental AI imaging tool. Moderate equivalence dependency. Overall, this clearance reflects a predicate-aligned approval typical of modern AI radiology extensions - not a novel clinical breakthrough, but a validated iteration within an established regulatory category.

View all Eastman Kodak Company devices

Submission Details

510(k) Number K923270 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 06, 1992
Decision Date September 11, 1992
Days to Decision 67 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
40d faster than avg
Panel avg: 107d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LLZ System, Image Processing, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2050
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - LLZ System, Image Processing, Radiological

All 756
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K923270.
SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE
K935694 · Siemens Medical Solutions USA, Inc. · Mar 1994
PRESTILIX 1694 D IMAGE INTENSIFIED FLUOROSCCOPIC
K924310 · GE Medical Systems · Jan 1993
DU PONT LINX HD-25 LASR IMAGER
K923042 · E.I. Dupont DE Nemours & Co., Inc. · Nov 1992
INTEGRATED DIAGNOSTIC SYSTEM W/ADD'L OPTIONS
K902428 · GE Medical Systems · Nov 1990
KODAK EKTASCAN LASER PRINTER, MODEL 100 XLP
K904590 · Eastman Kodak Company · Nov 1990
IMAGE INTENSIFIED FLUOROSCOPIC X-RAY SYSTEM
K903196 · General Electric Co. · Aug 1990