Cleared Traditional

K922411 - KODAK EKTASCAN, XLT7720, XLT7700, PCD 2000

K922411 is an FDA 510(k) clearance for KODAK EKTASCAN, manufactured by Eastman Kodak Company. The device is a Class 2 Radiology device with product code LMC cleared through the Traditional 510(k) pathway after a 95-day FDA review.

K922411 · Eastman Kodak Company · Radiology device
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Aug 1992
Decision
95d
Days
Class 2
Risk

K922411 is an FDA 510(k) clearance for the KODAK EKTASCAN, XLT7720, XLT7700, PCD 2000. Classified as Camera, Multi Format, Radiological (product code LMC), Class II - Special Controls.

Submitted by Eastman Kodak Company (Rochester, US). The FDA issued a Cleared decision on August 24, 1992 after a review of 95 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2040 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Eastman Kodak Company devices

FDA 510(k) Submission Details - K922411

510(k) Number K922411 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 21, 1992
Decision Date August 24, 1992
Days to Decision 95 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
12d faster than avg
Panel avg: 107d · This submission: 95d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LMC Device Classification - Class 2, Special Controls

Product Code LMC Camera, Multi Format, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2040
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 - LMC Camera, Multi Format, Radiological

All 73
Devices cleared under the same product code (LMC) and FDA review panel - the closest regulatory comparables to K922411.
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