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: LJF FDA class 1

Device, Antimicrobial Drug Removal

Microbiology

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An antimicrobial drug removal device is a microbiology laboratory tool used to neutralize or remove residual antimicrobial agents from patient blood or other specimens prior to culture, preventing antibiotic carryover from inhibiting bacterial growth and thereby improving the sensitivity of microbiological cultures. The device is FDA Class 1, the lowest risk category, requiring only general controls and exempt from premarket notification. It carries product code LJF and is regulated under 21 CFR 866.2560 within the Microbiology specialty. No special flags apply to this device.

510(k) Clearances

4 matches
K Number
Device Name
BACT/ALERT CSR
ARTIMICROBIAL REMOVAL DEVICE
BACTEC 170 TRYPTIC SOY BROTH W/RESINS
ANTIMICROBIAL REMOVAL DEVICE (ARD)

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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