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: IEO FDA class 1

Processor, Tissue, Automated

Pathology

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An automated tissue processor is a laboratory instrument used in histopathology to carry out the sequential dehydration, clearing, and paraffin infiltration steps necessary to prepare excised tissue specimens for embedding and microtome sectioning, replacing manual processing. It is regulated as an FDA Class 1 device, the lowest risk level, subject to general controls without requiring premarket notification. The product code is IEO, regulated under 21 CFR 864.3875, in the Pathology medical specialty.

510(k) Clearances

12 matches
K Number
Device Name
MICROWAVE AUTOMATED TISSUE PROCESSOR
LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)
SAKURA HEM-480 ELECTRON MICROSCOPY PROCESSOR
LX 300 TISSUE PROCESSOR
LX120 TISSUE PROCESSOR
LKB 2189 ULTROPROCESSOR
AUTOTECHNICON V TISSUE PROCESS SYS
TISSUE-TEK V.I.P. 100/200
TISSUE-TEK III MINI-RAPID PROCESSOR
TISSUE PROCESSING SYSTEM
TISSUE-TEK III V.I.P.
HISTO-TEK W/ AUTOMATIC COVERSLIPPER

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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