Cleared Traditional

K012010 - MODIFICATION TO LR 5200 FILM RECORDER

K012010 is an FDA 510(k) clearance for MODIFICATION TO LR 5200 FILM RECORDER, manufactured by Agfa Corp.. The device is a Class 2 Radiology device with product code LMC cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K012010 · Agfa Corp. · Radiology device
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Sep 2001
Decision
85d
Days
Class 2
Risk

K012010 is an FDA 510(k) clearance for the MODIFICATION TO LR 5200 FILM RECORDER. Classified as Camera, Multi Format, Radiological (product code LMC), Class II - Special Controls.

Submitted by Agfa Corp. (Rockville, US). The FDA issued a Cleared decision on September 20, 2001 after a review of 85 days - a notably fast clearance cycle.

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: 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 Agfa Corp. devices

FDA 510(k) Submission Details - K012010

510(k) Number K012010 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 27, 2001
Decision Date September 20, 2001
Days to Decision 85 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
22d faster than avg
Panel avg: 107d · This submission: 85d
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 55
Devices cleared under the same product code (LMC) and FDA review panel - the closest regulatory comparables to K012010.
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