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: MQG FDA class 2

Accessory, Assisted Reproduction

Obstetrics/Gynecology

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Accessories for Assisted Reproduction are obstetrics/gynecology devices used in conjunction with ART procedures to support gamete and embryo handling, transfer, and related steps in reproductive technology. Classified as FDA Class 2 under 21 CFR 884.6120, they require 510(k) premarket notification. The product code is MQG, and these accessories are eligible for third-party 510(k) review.

510(k) Clearances

45 matches
K Number
Device Name
Harioculture TL-16 Time-lapse Incubator
Embryo Real-time Incubator (TLS301), Embryo Real-time Culture Dish (MC 2004)
Geri Embryo Incubator with Geri Connect and Geri Assess Software, and Geri Dish
EmbryoScope+
Geri Embryo Incubator and Geri Dish
Geri Embryo Incubator and Geri Dish
COOK Vacuum Pump
RI Witness Embryology Heated Plate
MIRI TL
EMBRYOVIEWER SOFTWARE
Origio Gas Line Filter
XQ-1 INCUBATOR
PLANER BT37 INCUBATOR
EMBRYO VIEWER SOFTWARE
EMBRYOSCOPE
HEAL FORCE CO2 INCUBATOR
EMBRYOSCOPE AND EMBRYOSLIDE
MINITUBE TEMPERATURE CONTROL UNIT SC-2000 + 2045
ZIVF-AIRE
KRYO ART CONTROLLED RATE FREEZER
BINDER CO2 INCUBATOR SERIE CB
CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES
KENDRO HERACELL 240 INCUBATOR
DB1 EMBRYO FREEZE
WORKBENCH BY <GENX>
THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476
PGD-PRE-IMPLANTATION GENETIC DIAGNOSTIC PIPETTES (BIOPSY PIPETTES)
SANYO CO2 INCUBATORS, MODELS NOS. MCO-17AC, MCO-17AIC, MCO-20AIC,AND MC0-175M
K-SYSTEMS CULTURE BAG SEALER AND CULTURE BAGS TYPE CBS-1 AND CB-01
MTG - MINITUB HEATED STAGE SYSTEMS
<GENX> CODA INCUBATOR CELLMATE
MINITUB MULTI-PURPOSE CASSETTES
RS BIOTECH GALAXY 'R' CO2 INCUBATOR
CBS STRAW
KENDRO HERACELL CO2 INCUBATOR
GENX CODA AIR PURIFICATION SYSTEM
FORMA SCIENTIFIC DIRECT HEAT INCUBATORS
CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT
COOK ULTRA QUIET VACUUM PUMP & REGULATOR
HOFFMAN IVF-1
FORMA SCIENTIFIC UNIVERSAL WATER-JACKETED INCUBATOR
THERMOPLATE
K-SYSTEMS WORK STATIONS, TYPE L-13W, L-13E, L-13ES, L-13ET, L-13EM, L-23, L-23E, L-24, L-24E, L-25, L-25E, L-26, L-26E,L
COOK MINI-INCUBATOR
COOK TEST TUBE HEATER

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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