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: KZE FDA class 2

Injector, Fluid, Non-Electrically Powered

General Hospital

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The Non-Electrically Powered Fluid Injector is a mechanical device that uses manual or pneumatic force to inject fluids into patients without reliance on an electrical power source, used in settings where controlled fluid delivery is needed without powered equipment. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification before marketing. The product code is KZE, regulated under 21 CFR 880.5430, in the General Hospital medical specialty. No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM
PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL 501-01, STRATIS INJECTOR CATALOG 501-10, STRATIS RESET STATI
PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEM
LECTRAJET NEEDLE-FREE INJECTION SYSTEM, MODEL: M3 RA
ZETAJET
PHARMAJET NEEDLE-FREE INJECTION SYSTEM
AIRGENT, MODEL AG7000010
COOL.CLICK 2
BIOVALVE MINI-JECT NEEDLEFREE INJECTOR
COOL.CLICK
GENESIS MEDICAL TECHNOLOGIES, INC. PHARMAJET NEEDLE-FREE INJECTOR, MODEL M2000
HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500
BIOVALVE MINIJECT NEEDLE-FREE INJECTION SYSTEM, MODEL FG-01-001
AVANT GUARDIAN 101
INJEX NEEDLE-FREE INJECTION SYSTEM; ROJEX NEEDLE-FREE INJECTION SYSTEM
INJEX 30 NEEDLE FREE INJECTION SYSTEM, MODEL 100000
INJEX 30 NEEDLE FREE INJECTION SYSTEM
BI-3M NEEDLE-FREE INJECTOR SYSTEM
JET SYRINGE MODEL-100500
SEROJET
INJEX 50 SYSTEM
CLICKER
MODIFICATION TO MEDI-JECT CORPORATION MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN DELIVERY SYSTEM
J-TIP NEEDLESS INJECTOR
J-TIP INJECTOR
BIOJECTOR 2000 MODEL 1B02000
VITAJET
MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN DELIVERY SYSTEM
MEDI-JECT CORPORATION MEDI-JECTOR NEEDLE-FREE BIO-TROPIN DDRUG DELIVERY SYSTEMS 0.0058/0.0068(INCH DIAMETER NOZZLEORIFIC
MEDIVAX
HYPEX(TM) JET INJECTOR
BIOJECT JET INJECTION SYSTEM
PRECI-JET 50
OPHTHALMIC VISCOINJECTOR DRIVE
MED-E-JET INJECTOR
INJECTOR, INSULIN
VITAJET(INSULIN JET INJECTION DEVICE)
J-TIP INJECTOR SYSTEM
DERATA MEDI-JECTOR V
ROBINJECT
BIOJECTOR SYRINGE SYSTEM
DERATA MEDI-JECTOR IV
INJET-100, FLUID INJECTOR
JECT-AID
MEDAJET XL - JET INJECTOR
DERATA MEDI-JECTOR PRO
VACUUM COMPRESSION INJECTOR
PRECI-JET 50
NEW VITAJET
DERATA MEDI-JECTOR III

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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