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: FLF FDA class 2

Sterilizer, Ethylene-Oxide Gas

General Hospital

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The Ethylene-Oxide Gas Sterilizer is a device used in healthcare settings to sterilize heat-sensitive medical instruments and materials using ethylene oxide gas, which kills microorganisms including spores. It is classified as FDA Class 2 (moderate risk) and requires 510(k) premarket notification. The product code is FLF, regulated under 21 CFR 880.6860 in the General Hospital specialty.

510(k) Clearances

26 matches
K Number
Device Name
EOGas 4 Ethylene Oxide Gas Sterilizer
Anprolene AN75 Ethylene Oxide Gas Sterilizer
EOGas 4 Ethylene Oxide Gas Sterilizer
3M STERI-VAC STERILIZER/AERATOR
TSO3 OZONE STERILIZER, MODEL 125L
TSO3 OZONE STERILIZER, MODEL 125L
TSO3 OZONE STERILIZER, MODEL 125L
H & W HOSPITAL ETHYLENE OXIDE STERILIZER CONTROL SYSTEM
STERRAD 50 & STERRAD 100S STERILIZERS
PLAZLYTE(TM)
ABTOX PLAZLYTE PROCESS MONITOR
STERI-VAC GAS STERILIZER MODEL 8XL
THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZER
STERRAD 100 STERILIZATION SYSTEM
MDT/CASTLE 10/90 DUAL LOAD STATION
MDT/CASTLE 10/90 LOAD STATION
JOSLYN EO STERILIZER/ EO MODERNIZATION KIT
STERI-VAC GAS STERILIZER MODEL 5XL
KARLSON OZONE STERILIZER MODEL 100B
ARS ENTERPRISES ETHYLENE OXIDE GAS STERILIZER
ETHYLENE OXIDE GAS STERILIZA SYS II
EAGLE 2000 STERILIZER SERIES GAS/AERA
GAS STERILIZATION EQUIPMENT
CASTLE MICROCOMPUTER STERILIZER CONTROL
STERI-VAC #400C GAS STERILIZER
1500 EO EXHAUST HOOD

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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