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: CCQ FDA class 1

Nebulizer, Medicinal, Non-Ventilatory (Atomizer)

Anesthesiology

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The Non-Ventilatory Medicinal Nebulizer (Atomizer) is an anesthesiology device that generates a fine aerosol mist from liquid medications for inhalation by spontaneously breathing patients, not intended for use in-line with mechanical ventilation circuits. It is classified as FDA Class 1 (lowest risk), subject only to general controls, and is exempt from premarket notification. The product code is CCQ, regulated under 21 CFR 868.5640, within the Anesthesiology medical specialty. No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
EZ SPRAY
E-Z SPACER MASK (SMALL)
MDI TUTOR
MEDSHIELD/AEROCHAMBER
SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-100
SALINE SOLUTION- STERILE
MODIFIED AEROCHAMBER WITH MASK
MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER
FRANK INHALER THERMAL S
EVOLUTION ULTRASONIC
PARI INHALIERBOY TYPE 37.80 DOUBLE INSULATED
PFEIFFER METERED DOSAGE SYSTEM
FREEWAY NEBULIZER COMPRESSOR
DEVILBISS MODEL 6610D
DEVILBISS MODEL 8500D AND 8500D-608
GENTLEHALER(R)
DEY-PAK PURIFIED WATER, USP, STERILE
DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USP
MONAGHAN AEROCHAMBER WITH MASK
INSPIREASE(R), DRUG DELIVERY SYSTEM
INTERMITTENT SIGNAL ACTUATED NEBULIZER (VISAN)
MISTMASTER
THE SPIRA ELEKTRO 2
PREFILLED RESPIRATORY THERAPY VIALS
HAND HELD PHEUMATIC POWERED (DISPOSABLE) NEBULIZER
CHALLENGER DOSIMETER
ROSENTHAL-FRENCH NEBULIZATION DOSIMETER
CIRRUS DRUG NEBULIZER MK III
CIRRUS NEBULIZER-DELUXE KIT
MEDIPART REMOTE INJECTION SYS FOR ULTRAVENT RADIOA
MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S
PULMO-AIDE MODEL 5610D
MAXI-NEB
MEDIX ELECTRONIC NEBULIZING SYSTEM
SYNCHRONER TM (PROPOSED TRADENAME)
PFEIFFER PUMP
MICRO-INHALER MODEL TV-7000 & TV-8000
MICRON ONE PORTA. ULTRASONIC NEBULIZER
MIST-EASE NEBULIZER
AVA-NEB NEBULIZER
VMT GENTLE-HALER
ARM-A-VIAL LV STERIAL WATER FOR INHALA
ARM-A-CARE NEBULIZER-NEBULIZER
ARM-A-VIAL LV SODIUM CHLORIDE INHALAT
ARM-A-VIAL LV SODIUM, CHLORIDE INHALAT
ARM-A-CARE HUMIDIFIER-RESPIRATORY GAS
CROUP TENT FRAME
VMT HAND HELD NEBULIZER
MISTY OX DISPOS. NEBULIZER
AIR-NEB NEBULIZER COMPRESSOR UNIT

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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