Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: LJG FDA class 1

Quality Control Slides

Microbiology

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Quality control slides are prepared microscopy slides containing fixed reference material used to verify the performance of staining procedures, microscopes, and laboratory personnel skills in microbiology and pathology laboratories, ensuring consistent and reliable diagnostic results. The device is FDA Class 1, the lowest risk category, requiring only general controls and exempt from premarket notification. It carries product code LJG and is regulated under 21 CFR 866.2660 within the Microbiology specialty. No special flags apply to this device.

510(k) Clearances

27 matches
K Number
Device Name
MICROSPORIDIUM CONTROL SET
MICROSPORIDIUM CONTROL SLIDE
CRYPTOSPORIDIUM CONTROL SLIDE
GRAM STAIN CONTROL SLIDE
BION DIRECT IDENTIFICATION CONTROL SLIDE
HISTO-CHECK ACID FAST SLIDES
HISTO-CHECK FUNGAL CONTROL SLIDES
HISTO-CHECK LEGIONELLA CONTROL SLIDES
HISTO-CHECK GRAM NEGATIVE SLIDES
HISTO-CHECK PARASITIC CONTROL SLIDES
HISTO-CHECK SLIDES
FUNGI HISTOLOGY CONTROL SLIDES
ACID FAST BACILLI HISTOLOGY CONTROL SLIDES
SPIROCHETES HISTOLOGY CONTROL SLIDES
LEGIONELLA PNEUMOPHILLA HISTOLOGY CONTROL SLIDES
PNEUMOCYSTIS CARINII HISTOLOGY CONTROL SLIDES
INTRACELLULAR AMYLOID HISTOLOGY CONTROL SLIDES
INTRACELLULAR/EXTRACELLULAR IRON HISTOLOGY CONTROL
ATS CRYPTOSPORIDIUM STAIN CONTROL SLIDES
PROTOZOA STAIN CONTROL
METACHROMATIC GRANULE STAIN CONTROL
ACID FAST BACILLI STAIN CONTROL
Q-CHECK REAGENT STANDARDS
ATS GRAM STAIN CONTROL SLIDE
ATS AFB STAIN CONTROL SLIDE
ATS PARASITOLOGY STAIN CONTROL SLIDE
ACID FAST QUALITY CONTROL SLIDES

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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