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: JOY FDA class 2

Device, Automated Cell-Locating

Hematology

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The Device, Automated Cell-Locating is a hematology laboratory instrument designed to automatically identify and locate cells of interest on microscopy slides or within specimens, reducing the time required for manual scanning and assisting laboratory personnel in the review of hematological and cytological preparations. This device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification before marketing. It carries product code JOY and is regulated under 21 CFR 864.5260, within the Hematology medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

35 matches
K Number
Device Name
X100/X100HT with Full Field Peripheral Blood Smear (PBS) Application
AI100 with Shonit
X100HT with Slide Loader with Full Field Peripheral Blood Smear (PBS) Application
CellaVision DC-1, CellaVision DC-1 PPA
X100 with Full Field Peripheral Blood Smear (PBS) Application
Sysmex UD-10, Fully Automated Urine Particle Digital Imaging Device
Advanced RBC Application
CELLAVISION DM1200 WITH THE BODY FLUID APPLICTION
EASYCELL CELL LOCATOR
CELLAVISION DM1200 AUTOMATED HEMATOLOGY ANALYZER, MODEL XU-10127
CELLAVISION DM96 WITH THE BODY FLUID APPLICATION
SCANVIEW, MODEL SC-300
DUET SYSTEM
IKONISCOPE ONCOFISH BLADDER TEST SYSTEM
IKONISCOPE FASTFISH AUTO/AMNIOCYTE TEST SYSTEM
IKONISCOPE FASTFISH AMNIO IMAGING SYSTEM
MODIFICATION TO DUET SYSTEM
DUET SYSTEM
CELLAVISION DM96 AUTOMATIC HEMATOLOGY ANALYZER
DUET SYSTEM
DIFFMASTER OCTAVIA AUTOMATIC HEMATOLOGY ANALYZER
SLIDESCAN
AUTOMATED CELLULAR IMAGING SYSTEM (ACIS)
TRACCELL 2000 SLIDE MAPPING SYSTEM
MICRO21 WITH URINE SEDIMENT ANALYSIS
WINSCAN AUTOMATED IMAGING SYSTEM
MICRO21 WITH WBC ESTIMATE
MICRO21 WITH CEREBROSPINAL FLUID
TRACCELL 2000 SLIDE MAPPING SYSTEM
MDX 2000, DIGITAL ANALYZER
MICRO21 WITH ANA
MICRO21 WITH RETIC
IMS-200
RE-CELL SLIDE RECAP
SCANNING SYS., AUTO. COMP., ACS1000

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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