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: ONB FDA class 2

Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System

General Hospital

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The Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System (product code ONB) is a Class 2 device regulated under 21 CFR 880.5440 in the General Hospital specialty (HO), cleared via 510(k). It is designed to reconstitute and transfer antineoplastic and other hazardous drugs in healthcare settings to reduce exposure of healthcare personnel to chemotherapy agents during drug preparation and administration. The device is not an implant and is not life-sustaining.

510(k) Clearances

37 matches
K Number
Device Name
ProSeal™ Bag Spike with Additive Port (423370ST, 423370)
ZeroClear™ Bag Access (423100)
ProSeal™ Vented Universal Vial Adaptor
ProSeal™ Closed System Bag Access
ProSeal™ In Line Pump Set (423850)
ToxiSeal™ Vial Adaptor
ToxiSeal™ Vial Adaptor with External Flip Balloon
ProSeal™ Injection Site Extended Male Luer Lock (422140)
ProSeal™ Injector Plus (Model no. 421050)
ToxiSeal Vial Adapter with External Balloon
Chemfort® Catheter Adaptor
BD Texium™ Closed Male Luer
Equashield Closed System Transfer Device
Closed System Transfer Device
OnGuard2 Chemfort Closed Administration (CADM)
Arisure Closed System Drug Transfer Device (CSTD)
TEVADAPTOR Bag Adaptor LL, TEVADAPTOR Bag Adaptor LL with ULTRASITE, TEVADAPTOR Bag Adaptor SP with ULTRASITE, TEVADAPTOR IV Secondary Safety Set with ULTRASITE, TEVADAPTOR IV Secondary Safety set
BD PhaSeal Optima Closed System Drug Transfer Device
ProSeal™ Closed System drug Transfer Device (CSTD)
Chemfort CSTD
Diana ChemoClave Transfer Set
BD PhaSeal Optima Closed System Transfer Device
TEVADAPTOR Closed Drug Reconstitution and Transfer System
ChemoCLAVE Cytotoxic Medication Preparation and Delivery System
Halo Closed Vial Adaptor (Multiple Models based on 13, 20 or 28mm Vial Neck Size), Halo Closed Syringe Adaptor, Halo Closed Line Adaptor, Closed Vial Adaptor
Diana Medication Transfer Set
NEOSHIELD
Equashield Closed System drug Transfer Device (CSTD)
TEVADAPTOR Closed Drug Reconstitution and Transfer System
Equashield Closed System drug Transfer Device (CSTD)
Halo
TEVADAPTOR CLOSED DRUG RECONSTITUTION AND TRANSFER SYSTEM
BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - INJECTOR
EQUASHIELD CLOSED SYSTEM DRUG TRANSFER DEVICE (CSTD)
CHEMOLOCK, CHEMOLOCK PORT
BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - P55
BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE

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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