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: POV FDA class 2

Semen Analysis Device

Hematology

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The Semen Analysis Device (product code POV) is a Class 2 hematology device used to evaluate one or more human semen parameters including semen volume, sperm concentration, total sperm number, sperm motility, sperm morphology, sperm vitality, white blood cell concentration, and pH, regulated under 864.5220. It requires 510(k) clearance. The device is not an implant and is not life-sustaining.

510(k) Clearances

27 matches
K Number
Device Name
LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer
LensHooke X12 PRO Semen Analysis System
SQA-iOw Sperm Quality Analyzer
YO Home Sperm Test
SQA-iO Sperm Quality Analyzer
LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SE Semen Quality Analyzer
SwimCount Sperm Quality Test
LensHooke X1 Pro Semen Quality Analyzer, LensHooke X1 Semen Quality Analyzer
Trak Plus Male Fertility Testing System
YO Home Sperm Test
Trak Male Fertility Testing System
SPERMCHECK FERTILITY
SPERMCHECK VASECTOMY
GENERAL SEMEN ANALYSIS KIT
QWIKCHECK TEST STRIPS- REAGENT STRIPS FOR SEMEN ANALYSIS
FERTELL MALE FERTILITY TEST
HBA SPERM-HYALURONAN BINDING ASSAY
GENERAL SEMEN ANALYSIS (GSA) KIT
SQA V, SPERM QUALITY ANALYZER
AUTOMARQER
SQA, SPERM QUALITY ANALYZER
FERTILMARQ HOME DIAGNOSTIC SCREENING TEST KIT FOR MALE INFERTILITY
AUTOMARQER
FERTILMARQ TEST KIT
SEMEN ANALYSIS KIT
SQA
CTS-3060 AUTOMATED SEMEN ANALYZER

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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