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: LIB FDA class 1

Device, General Purpose, Microbiology, Diagnostic

Microbiology

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A general-purpose microbiology diagnostic device encompasses a broad range of instruments, reagents, and accessories used in clinical microbiology laboratories for general diagnostic purposes, including culture media, inoculation tools, and other non-specific laboratory aids. The device is FDA Class 1, the lowest risk category, requiring only general controls and not requiring premarket notification. It bears product code LIB and is regulated under 21 CFR 866.2660 within the Microbiology specialty. No special flags apply to this device.

510(k) Clearances

43 matches
K Number
Device Name
OSMETECH MICROBIAL ANALYSER-BACTERIAL VAGINOSIS (OMA-BV)
SUPPLEMENTARY REAGENTS FOR ENZYGNOST/TMB
GULL ELISAWARE
CORNING EASY WASH ELISA PLATES
CELL LIFTER
NORMAL SALINE STERILE
CORNING ELISA PLATES
MICROSCOPE SLIDES
AUTO MASH
MINI MASH 2000
MULTI MASH 2000
IMMULON 1 EIA TUBES, IMMULON 2 EIA TUBES
MYWASHER 5
MIC-CONCEPT VIEWBOX
QUADRA TITER MICRO PLATES
PORTABLE DIAGNOSTIC LABORATORY
RAPID DIAGNOSTIC KIT
HAND-HELD SLIDE READER
PHARMA-PLAST PETRI DISH
GIARDIA GUARD
MACLEAN-FOGG, DISPOS-INOCULA-LOOPS
CODE-A-WELL SERIES 200 PLATE
CODE-A-WELL SERIES 300 PLATE
CODE-A-WELL
HCC-MYCOBACTERIA STAIN KIT
READER MICROELISA SYSTEM
IMMULON SUBSTRATE REMOVAWELL STRIPS
HEATING BLOCK MICROELISA SYSTEM
STRIPREADER MICROELISA SYSTEM
MICROELISA COMP
SPIA SYS FOR SOLID PHASE IMMUNOASSAYS
DISPOSABLE STERILE FILTER SYSTEM
HANDI-WASH
MICRO STIX #011-010-5000 & HOLDER#5100
REMOVAWELL PLATE LID
MICROFLUOR B PLATE & MICRO FLUOR W PLATE
MICROFLUOR B REMOVAWELL STRIPS
DISPOSABLE DISPENSING-SPREAD PIPETS
CALI-PIPETTE
CALI-LOOP
MINIWASH II
TEK-PRO TEK-TATOR V ROTATOR & HUMIDIFY
PROPOSED CONTROLS FOR DOSIMETRIC RELEASE

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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