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: FKR FDA class 2

Subsystem, Proportioning

Gastroenterology, Urology

View full classification →

The Proportioning Subsystem is a component of a hemodialysis delivery system responsible for accurately mixing concentrate with purified water to achieve the correct dialysate composition. It is classified as FDA Class 2 (moderate risk) and requires 510(k) premarket notification. The product code is FKR, regulated under 21 CFR 876.5820 in the Gastroenterology and Urology specialty. This device is designated as life sustaining or life supporting.

510(k) Clearances

12 matches
K Number
Device Name
NXSTAGE PUREFLOW SL
NXSTAGE PUREFLOW SL
NXSTAGE PUREFLOW SL
NXSTAGE DIALYSATE PREPARATION MODULE
NXSTAGE DIALYSATE PREPARATION MODULE, MODEL NX0269
SARTORIUS AQUASART SM 40035 - DIALYSATE SYS
AUTO-D AUTOMATIC DISINFECTION ACCESS/ATTACHMENTS
CHEMATIC BICARBONATE DIALYSATE SYSTEM
GAMBRO BICARBONATE MODULE, BCM-10
BICARB-O-MATE HEMODIALYSIS SOD. BICARB.
MOD. DM-357 BICARBONATE RETROFIT KIT
BIO-PRO UNIT

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