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: FLG FDA class 1

Cleaner, Ultrasonic, Medical Instrument

General Hospital

View full classification →

The Medical Instrument Ultrasonic Cleaner is a device that uses ultrasonic energy to remove debris and contaminants from surgical instruments and medical devices prior to sterilization or disinfection. It is classified as FDA Class 1 (lowest risk) and is subject only to general controls. The product code is FLG, regulated under 21 CFR 880.6150 in the General Hospital specialty.

510(k) Clearances

19 matches
K Number
Device Name
KLENZYME
ALSA-KLENZ
BILL EVANS-KLENZ
NPH-KLENZ
MON-KLENZ
INSTRU KLENZ
PDS ULTRACLEAN
SURGICLEAN ENZYMATIC INSTRUMENT CLEANER
INSTRUMENT DETERGENT CONCENTRATE
BIOSONIC ULTRASONIC CLEANING SYSTEM
RAPIDEX BIOLOGICAL SURFACTANT
UCS-2, ULTRASONIC CLEANING SOLUTION
WECK INSTRUMENT CLEANER, CAT. NO. 850-103
WEC-WASH, CATALOG NO. 850-115
WEC-KLEEN, CATALOG N. 850-102
WECK CONCENTRATED LIQUID CLEANER
SATALEC SEPTOSONIC SC 80/SC 120
CUSTOM ULTRASONICS-SYS 80, 81-24, 83-2
MICROFLATOR

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.

Popular Product Codes

Commonly searched