Cleared Traditional

KODAK LANEX MED. SCREEN (K792123) - FDA 510(k) Clearance

Class I Radiology device.

K792123 · Eastman Kodak Company · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1979
Decision
46d
Days
Class 1
Risk

K792123 is an FDA 510(k) clearance for the KODAK LANEX MED. SCREEN. Classified as Screen, Intensifying, Radiographic (product code EAM), Class I - General Controls.

Submitted by Eastman Kodak Company (Mchenry, US). The FDA issued a Cleared decision on December 10, 1979 after a review of 46 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1960 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Eastman Kodak Company devices

Submission Details

510(k) Number K792123 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 25, 1979
Decision Date December 10, 1979
Days to Decision 46 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 107d · This submission: 46d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EAM Screen, Intensifying, Radiographic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.1960
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - EAM Screen, Intensifying, Radiographic

All 18
Devices cleared under the same product code (EAM) and FDA review panel - the closest regulatory comparables to K792123.
CRONEX SR-337
K834484 · E.I. Dupont DE Nemours & Co., Inc. · Feb 1984
KODAK INTENSIFYING SCREEN 80-175
K813147 · Eastman Kodak Company · Dec 1981
KODAK INTENSIFYING SCREEN SO-168
K813139 · Eastman Kodak Company · Dec 1981
SCREEN, FINE, LANES, KODAK
K770837 · Eastman Kodak Company · May 1977
CRONEX QUANTA III INTENSIFYING SCREENS
K770574 · E.I. Dupont DE Nemours & Co., Inc. · Apr 1977
FLUORICON 500 IMAGE INTENSIFIERS
K770094 · General Electric Co. · Jan 1977