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: MNT FDA class 2

Ventilator, Continuous, Minimal Ventilatory Support, Facility Use

Anesthesiology

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The Continuous Ventilator for Minimal Ventilatory Support (Facility Use) is a respiratory device intended for use in clinical facilities to provide minimal, continuous ventilatory support to patients. Classified as FDA Class 2 under 21 CFR 868.5895 in the Anesthesiology specialty, it requires 510(k) premarket notification. The product code is MNT, and it carries a life-sustaining support flag, indicating it is used to sustain patient life.

510(k) Clearances

24 matches
K Number
Device Name
HFT750U
Vivo 3
F&P Airvo 3 NIV (PT311US)
Servo-air Lite Ventilator System
Nihon Kohden NKV-330 Ventilator System
F&P Nivairo RT047 Vented Hospital Full Face Mask, Anti-Asphyxiation Valve Version
Nivairo RT045 Non-Vented Hospital Full Face Mask Anti-Asphyxiation Valve - Large, Nivairo RT045 Non-Vented Hospital Full Face Mask Anti-Asphyxiation Valve - Medium, Nivairo RT045 Non-Vented Hospital Full Face Mask Anti-Asphyxiation Valve - Small, Nivairo RT045 Non-Vented Hospital Full Face Mask Anti-Asphyxiation Valve - Extra Small
STELLAR 150
BIPAP A 40 VENTILATORY SUPPORT SYSTEM
STELLAR 150
V60 VENTILATOR WITH PPV AND AUTO-TRAK+ SOFTWARE OPTIONS
STELLAR 150
BREAS VIVO 40 SYSTEM
V60 VENTILATOR, MODEL V8000
BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 40
ACUTE CARE FACE MASK, MODEL RT040
BREAS VIVO 40 SYSTEM
KNIGHTSTAR 330 VENTILATOR
STICK-ON DISPOSABLE NASAL MASK, MODEL 312174, 1001964
BIPAP VISION VENTILATORY SUPPORT
SULLIVAN VPAP II ST VENTILATORY SUPPORT SYSTEM
KNIGHTSTAR 335
BIPAP S/T-D 30 SYSTEM
BIPAP MODEL S/T-D

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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