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: DTQ FDA class 2

Console, Heart-Lung Machine, Cardiopulmonary Bypass

Cardiovascular

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The Heart-Lung Machine Console for Cardiopulmonary Bypass is a life-sustaining cardiovascular device that integrates and controls the pumps, alarms, and monitoring functions of an extracorporeal circulation system, maintaining blood flow and gas exchange for the patient during open-heart surgery. It is classified as an FDA Class 2 device, indicating moderate risk, and requires 510(k) premarket notification before marketing. The product code is DTQ and it is regulated under 21 CFR 870.4220 within the Cardiovascular medical specialty. This device is designated as life-sustaining or life-supporting.

510(k) Clearances

50+ matches
K Number
Device Name
Essenz HLM, Essenz ILBM
Terumo Advanced Perfusion System 1
Essenz HLM
Stockert S5 System
Century Perfusion System
Quantum Smart Occluder LH (left-hand), Quantum Smart Occluder LH (right-hand)
Quantum Pump Console
Advanced Perfusion System 1
Advanced Perfusion System 1
Advanced Perfusion System 1
Advanced Perfusion System 1
CARDIOHELP SYSTEM
ADVANCED PERFUSION SYSTEM 1
CARDIOHELP SYSTEM
SORIN C5 SYSTEM; 85/C5 MAST ROLLER PUMP SYSTEM 150(1X RP 150 AND CONTROL PANEL WITH CONNECTING CABLES); S5/C5 MAST ROLLE
SORIN C5 SYSTEM MODEL 58-00-00
SORIN B-CARE5 FOR THE STOCKERT S5 SYSTEM
LIFEBRIDGE B2T, MODEL 7001
AIR PURGE CONTROL SYSTEM FOR S5 SYSTEM MODEL 23-45-05
STOCKERT S5 SYSTEM, STOCKERT GAS BLENDER
MODIFICATION TO: STOCKERT S5 SYSTEM
PERFORMER CBP SYSTEM
MODIFICATION TO STOCKERT S5 SYSTEM
STOCKERT S5 SYSTEM
MEDTRONIC PERFORMER TM CPB, MODEL R51, PCPB
ADVANCED PERFUSION SYSTEM 1 (100/120 VOLT),ADVANCED PERFUSION SYSTEM 1 (220/240 VOLT, ROLLER PUMPS (6, 4 INCH
MODIFICATION TO CARDIOVENTION POWERBASE CONSOLE, MODEL PCB-100
CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100
STOCKERT CENTRIFUGAL PUMP CONSOLE
SIII ALARM AMPLIFIER
S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0
STOCKERT COMPACT SYSTEM VERSION 2.0
STOCKERT COMPACT SYSTEM
AFFINITY BLOOD PUMP SYSTEM
JOSTRA HL-20 INTEGRATED PERFUSION SYSTEM
STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE
SORIN BLOOD CARDIOPLEGIA CONSOLE
SARNS 8000 MODULAR PERFUSION SYSTEM
SARNS 9000 HEART-LUNG CONSOLE
ONGUARD 1000, CATALOG #043611-000 & 043611-001
STOCKERT-SHILEY CAPS BATTERY MODULE
STOCKERT-SHILEY CAPS HLM INTERFACE
STOCKERT-SHILEY CAPS TIMER MODULE
SARNS PORTABLE POWER MODULE
CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE
CENTRIMED SYSTEM 1 W/24 VOLT BATTERY POWER SUPPLY
COBE EMERGENCY POWER SOURCE 43610-000
GAMBRO PUMP CONSOLE CSL
POLYSTAN HEART LUNG MACHINE SYS
SARNS 7000 MONITOR MODULE

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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