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: KPE FDA class 2

Container, I.V.

General Hospital

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This device is an intravenous (I.V.) container used to hold and deliver fluids, medications, or parenteral nutrition to patients via intravenous infusion. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket notification. The product code is KPE, regulated under 21 CFR 880.5025 within the General Hospital specialty. This device is eligible for third-party review as part of the 510(k) process.

510(k) Clearances

50+ matches
K Number
Device Name
DMRX 100ml Empty Container Solution; DMRX 250ml Empty Container Solution; DMRX 500ml Empty Container Solution; DMRX 1000ml Empty Container Solution
eZSURE™ Empty Fluid Container with ProSeal™ Injection Site
eZSURE™ Empty Fluid Container (models 426030, 426040, 426110)
Disposable Infusion Bag for Parenteral Nutrition
Empty EVA Bag
SmartSite Bag 500mL, SmartSite Bag 250 mL, SmartSite Bag 100 mL
Empty EVA Bag
HCT Empty EVA Container Pack
Additive Cap
Empty Eva Bag, models FVM0134BP, FVM0135BP, FVM0136BP, FVM0137BP, FVM0138BP, FVM0139BP, FVM0140BP, FVM0141BP
STERILE EMPTY GLASS CONTAINER, 250ML, STERILE EMPTY GLASS CONTAINER, 500 ML, STERILE EMPTY GLASS CONTAINER, 1000 ML
EMPTY EVA SOLUTION CONTAINER EMPTY EVA DUAL CHAMBER SOLUTION CONTAINER
ADDITIVE CAP
EVA TPN BAG
ALL-IN-ONE CONTAINER
DUAL CHAMBER TPN CONTAINER
KAWASUMI LABORATORIES EMPTY SOLUTION CONTAINER
CHURCHILL MEDICAL DUAL CHAMBER EMPTY CONTAINER
EVA TPN CONTAINER
GRI-BAG, GRI-BAG AP
GRI-FLEX, MODELS 1000ML, 500ML, 250ML, 100ML
EVA EMPTY SOLUTION CONTAINER
ALL-IN-ONE TWO CHAMBER CONTAINER 3200 ML, 2000 ML & 1000 ML
TPN NUTRITION BAG (EVA), EMPTYING TUBE, BAG SYRINGE FILL SET
EMPTY RESERVOIR BAG, 50 ML,100 ML,250 ML,500 ML, 1000M ML, 1500 ML, 2000 ML, 3000 ML
ALL-IN-ONE CONTAINER CAT#'S 2B8114,2B8124, 2B8134, 2B8144, 2B8102, 2B8152, 2B8112, 2B8117M 2B8122, 2B8132, 2B8142, 2B712
MPS RESERVOIR BAG
STERI-TAMP
CHARTERMED TPN-EVA BAGS
VITALMIX PLUS EMPTY I.V. CONTAINER
INTRAVIA CONTAINER, EMPTY
SECURE EVA DUAL CHAMBER MIXING BAG
ALL-IN-ONE TWO CHAMBER CONTAINER
EMPTY, SOLUTION TRANSFER CONTAINER WITH DETATCHABLE LEG SET
UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET
DISPOSABLE BAG DECANTER
SOLUTION TRANSFER CONTAINER W/ATTACHED LEG SET (EMPTY)
PHARMAFEED
EVA EMPTY MIXING CONTAINER
EMPTY MIXING CONTAINER
DUAL CHAMBER MIXING BAG
EMPTY SOLUTION TRANSFER CONTAINER W/ DETACH LEG
EMPTY VIAFLEX PLASTIC CONTAINER
SNAPPER
DUAL COMPARTMENT TPN BAG 3 LITER
EMPTY I.V. CONTAINER
CHEMOTHERAPY CONTAINER
BAG SPIGOT
ADMIXTURE CONTAINER FOR TOTAL PARENTERAL NUTRITION
CHARTERMED EMPTY TPN CONTAINER - 100 ML CAPACITY

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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