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: MRZ FDA class 2

Accessories, Pump, Infusion

General Hospital

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Accessories for Infusion Pumps are supplementary components designed to support the operation of infusion pump systems used in clinical settings for the controlled delivery of fluids, medications, or nutrients to patients. These accessories fall under FDA Class 2 (510(k)), meaning manufacturers must demonstrate substantial equivalence to a predicate device before marketing. The product code is MRZ, regulated under 21 CFR 880.5725, and overseen by the General Hospital medical specialty panel. This device is not classified as an implant and does not have life-sustaining or life-supporting designation.

510(k) Clearances

48 matches
K Number
Device Name
UTC 3mL Medication Cartridge
Elite Biomedical Solutions Dose Request Cord
RG 3ml Medication Cartridge
BlueStar Rx
SpaceStation MRI
WellDoc BlueStar
Lockbox for Perfusor Space PCA Infusion Pump
Sapphire Sets
WellDoc BlueStar, WellDoc BlueStar Rx
Hospira Sapphire Sets
WellDoc BlueStar (WellDoc DiabetesManager System and DiabetesManager-Rx System
ivWatch Model 400
SMART LABEL, PROPOFOL
WELLDOC DIABETESMANAGER SYSTEM AND DIABETESMANAGER- RX SYSTE
ONETOUCH REVEAL
PATIENT CONTROLLED ANALGESIA (PCA) BUTTON CABLE
WELLDOC DIABETES MANAGER SYSTEM AND DIABETES MANAGER RX SYSTEM
WELLDOC DIABETES MANAGER SYSTEM AND DIABETES MANAGER RX SYSTEM
AIDERA DIASEND SYSTEM
DIABETESMANAGER SYSTEM, DIABETESMANAGER-RX SYSTEM MODEL VERSION 1.1
LOCKBOX FOR USE WITH MEDFUSION 3000 SERIES PUMPS
AIDERA DIASEND
CADD -SOLIS MEDICATION SAFETY SOFTWARE: ADMINISTRATOR AND POINT-OF-CARE
ACCU-CHEK 360 DIABETES MANAGEMENT SYSTEM
EZ MANAGER MAX DIABETES MANAGEMENT SOFTWARE
CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE-ADMINISTRATOR (21-6275), POINT OF CARE (21-6276)
MEDTRONIC MINIMED CARELINK USB CONNECTOR, MODEL NMT 7305
DANA 3CC SYRINGE INSULIN RESERVOIR
HOSPIRA GEMSTAR INFUSION PUMP SYSTEM WITH HOSPIRA GEMSTAR SPRING ASSIST MECHANISM LOCKBOX-7 THERAPY
RITA CLIPS FOR INFUSION PUMPS
PREPARE CARTRIDGE
MEDTRONIC MINIMED COMLINK, HARDWARE MODEL 7304 & SOFTWARE MODEL 7311
BAXTER AS40A, AS41 SYRINGE PUMP, MODEL N61WC
MEDFUSION 2001 & 2010, MODEL N7215IWC
SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2
S.P.A.R STERILE AMBULATORY RESERVOIR
INFUTEST 2000 INFUSION DEVICE ANALYZER
IVAC MEDSYSTEM III, INFUSION PUMP W/DRUG EDITING SOFTWARE KIT
THE HARVARD LIBRARY
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS3030-P
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL625
STERILE AMBULATORY RESERVOIR 60ML/100ML
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS06224
ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M7)
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL825
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL8108
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018

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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