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: MNS FDA class 2

Ventilator, Continuous, Non-Life-Supporting

Anesthesiology

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The Continuous Non-Life-Supporting Ventilator is a respiratory device designed to provide continuous ventilatory support to patients who do not rely on the device for survival, typically used for comfort or mild respiratory support. Classified as FDA Class 2 under 21 CFR 868.5895 in the Anesthesiology specialty, it requires 510(k) premarket notification. The product code is MNS.

510(k) Clearances

44 matches
K Number
Device Name
Vivo 1, Vivo 2
ReddyPort Elbow
BPAP System
ReddyPort NIV Access Elbow
Juno VPAP ST-A
VPAP Adapt SV, VPAP Tx, S9 VPAP Tx
Juno VPAP ST-A
EASYCARE ONLINE
S9 VPAP TX
EASYCARE ONLINE
VPAP S-A
VPAP TX
VPAP ST-A
RESSCAN
BIPAP A 30 VENTILATORY SUPPORT SYSTEM
VPAP TX
OXIMETRY INTERFACE KIT
BIPAP AVAPS VENTILATORY SUPPORT SYSTEM
BIPAP SYNCHRONY 2 WITH AF531 FULL FACE MASK
VPAP III ST-A
DEVILBISS INTELLIPAP/ SLEEPCUBE BILEVEL ST, DV56 ST SERIES
BIPAP AVAPS VENTILATORY SUPPORT SYSTEM
VPAP TX
BIPAP AUTOSV ADVANCED
BIPAP SYNCHRONY 2
BIPAP AUTOSV
BIPAP SYNCHRONY 2 VENTILATORY SUPPORT SYSTEM
BIPAP SYNCHRONY WITH AVAPS
BIPAP AUTOSV
BIPAP SYNCHRONY
BREAS VIVO BILEVEL SYSTEM, MODEL VIVO 30
VPAP III ST-A/KIDSTA MASK SYSTEM
BIPAP FOCUS
VPAP ADAPT
VPAP III ST-A
NASAL-AIR CRITICAL CARE
BIPAP HARMONY VENTILATORY SUPPORT SYSTEM
BIPAP SYNCHRONY VENTILATORY SUPPORT SYSTEM WITH BI-FLEX
BIPAP SYNCHRONY VENTILATORY SUPPORT SYSTEM
BIPAP SYNCHRONY HC
BIPAP HARMONY S/T, MODEL 1001445
SULLIVAN VPAP II ST-A NASAL VPAP SYSTEM
MODEL 7700 QUANTUM PRESSURE SUPPORT VENTILATOR PSV
PURITAN-BENNETT 335 RESPIRATORY SUPPORT SYSTEM

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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