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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: KPA FDA class 1

Slide Stainer, Automated

Pathology

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This device is an automated slide stainer used in pathology laboratories to apply histological and cytological stains to tissue or cell specimens on microscope slides, enabling visualization under a microscope. It is classified as FDA Class 1, indicating low risk and requiring only general controls. The product code is KPA, regulated under 21 CFR 864.3800 within the Pathology specialty. No special flags apply to this device.

510(k) Clearances

21 matches
K Number
Device Name
PROFIBLOT
VERSABLOT
WESCOR MODEL 7300 AEROSPRAY GRAM STAINER
LX-100 SLIDE STAINER
WESBLOT PROCESSOR
SAKURA DRS-60 AUTOMATIC SLIDE STAINER
HISTOMATIC SLIDE STAINER, CODE-ON VERSION
MST-1050-II X-RAY UNIT
PUMP TUBE SETS FOR HEMA-TEK I & II SLIDE STAINERS
CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERS
MIDAS II AUTOMATIC STAINER
WESCOR 7100 AEROSPRAY SLIDE STAINER
MIDAS 6000 AUTOMATIC STAINER
MI DAS 1000 AUTOMATIC SLIDE STAINER
GUAMSTAINER
TECHNICON AUTOSLIDE STAINING/PROCESSING
HEMATOLOGY SLIDE STAINER
AUTO. SLIDE STAINER
CARA-STAIN MODEL 3000
HEMA-TEK II SLIDE STAINER
BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK

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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