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: BZR FDA class 2

Mixer, Breathing Gases, Anesthesia Inhalation

Anesthesiology

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The Mixer, Breathing Gases, Anesthesia Inhalation is a device that blends specified concentrations of anesthetic and non-anesthetic gases for delivery to a patient during inhalation anesthesia, allowing precise control over the inspired gas composition. It is classified as FDA Class 2, requiring 510(k) premarket notification. The product code is BZR, regulated under 21 CFR 868.5330 in the Anesthesiology specialty. This device is designated as life-sustaining or life-supporting and is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Midas Flowmeter; eAVS
Maxtec MaxBlend2+p
FlowStar Analog Mixer Flowmeter
FlowStar Touch Digital Mixer Flowmeter
Quality Mix Blender, Oxymixer
Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50
Equinox Advantage
MaxBlend 2, MaxBlend Lite
GMX Series Medical Air/Oxygen Blender
EQUINOX RELIEVE
MAXMIXING BLOCK
SEDARA GAS MIXER, SEDARA SCAVENGER MODEL: 03, 04
RESUSCITATION UNIT 105
HELIOX LOW FLOW SENTRY BLENDER
HELIO2 BLENDER
TENACORE OXYGEN BLENDER, MODEL TB-2000
PRECISION BLENDER
PRAXAIR MEDICAL AIR MIXER
CS MEDICAL TTCF GAS DELIVERY SYSTEM
SK MED ME202 MONITORING MIXER
SK MED M201 PLUS MIXER
SK MED M201 MIXER
MALLARD AIR OXYGEN ACCUBLENDER
SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIES
ALADDIN II MONITORING OXYGEN/AIR MONITOR
BIRD SENTRY BLENDER/ ANALYZER / BIRD SENTRY LOW FLOW BLENDER/ANALYZER
AIR OXYGE MIXER
ALADDIN MONITORING OXYGEN/AIR MIXER
AIR ENTRAINER 900RT008
OXY/STAR LOW FLOW BLENDER
PRIMA HYUPERINFLATION SYSTEM
BABYCARE NEO2 OXYGEN CONCENTRATION CONTROLLER
BMD AIR/OXYGEN BLENDER
MERIDIAN MEDICAL SYSTEMS HYPER INFLATION BAY SYST
PRECISION MED PRODUCTS LTD HYPERINFLATION SYSTEM
HYPERINFLATION SYSTEM
BIRD SENTRY AIR/OXYGEN MICROBLENDER
LOW FLOW N2O/02O MICROBLENDER
BIRD MICROBLENDER M.R.I.
NITRONOX(R), FIRST RESPONSE NITRONOX(TM)
P/N 9320 LOW FLOW AIR/OXYGEN MICROBLENDER
SIEMENS O2-AIR MIXER 965
LNI MGV MEDICAL GAS MIXER
THE M100 AIR/OXYGEN MIXER
OHMEDA OXYGEN BLENDER
SECHRIST AIR-OXYGEN MIXER & ANCILLARY
DOWNS CAP FLOW GENERATOR
SECHRIST SERIES 3500 AIR-OXYGEN MIXER
ROYAL
WINDSOR

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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