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: LHI FDA class 2

Set, I.V. Fluid Transfer

General Hospital

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An I.V. fluid transfer set is a tubing and connector assembly used in hospital settings to transfer intravenous fluids from one container to another or to prepare IV admixtures, facilitating safe and sterile fluid management during patient care. The device is FDA Class 2, indicating moderate risk and requiring 510(k) premarket clearance. It carries product code LHI and is regulated under 21 CFR 880.5440 within the General Hospital specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
Arisure® Closed Male Luer with Spike Adapter (YM060)
Rio™ Drug Reconstitution Transfer Device
SmartSiteTM Vented Vial Access Device
nextaro® va, 15mm, 5µm
Vent Vial Adapter
FlowArt Valve for Vial Access
Vial2Bag Advanced® 20mm Admixture Device
Vial Adapter with Filter
nextaro® v, 20/20
BD SmartSite™ 13mm Vial Access Device; BD SmartSite™ 20mm Vial Access Device
Mix2Vial® Transfer Device
Vial Adapter 20mm
Vial2Bag Advanced® 13mm Admixture Device
Vial Adapter
MixJect® Transfer Device
Vial Adapter
Vented Vial Transfer Pin
Vented Vial Adapter 20mm
Advcare Vial Direct to Bag (VDB) Needle-free Admixture Devices
Vial Adapter Ø13mm
freeflex+ Transfer Adapter
IVX Fluid Transfer Set
SOL-CARE IV Bag Safety Connector
B Dispensing Line
ProntoPump Sterile Tube Set
Mini Spike Plus 6/8R
Vial2Bag Advanced 20mm Admixture Device
Rio Vial-to-Bag Drug Reconstitution Device
Decanting Device
Vial Adapter Ø20 mm , Vial Adapter Ø13 mm
Vial Adapter Ø20 mm
nextaro Transfer System, nextaro va
Guarded Luer Connector
GRI-FILL PERISTALTIC SET
Vial Adapter 15mm
Arisure Closed Vial Adapter
Arisure Dry Spike
Vial2Bag Direct Connect
OnSite-IV
Vented Vial Adapter Transfer Device - 13mm
APEX Compounding System Transfer Set
KIRO Set
Universal Spike
SmartSite Vented Vial Access Device
VIAL-MATE Adaptor
VIAL2BAG DIRECT CONNECT
MEDSOURCE SELECTABLE IV SET
MEDSOURCE IV ADMINISTRATION SET 72 MEDSOURCE IV ADMINISTRATION SET, NEEDLELESS MALE ADAPTER, MEDSOURCE IV EXTENSION SET
E-Z LINK
ADD-VANTAGE ADDAPTOR

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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