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: MOD FDA class 2

Accessory To Continuous Ventilator (Respirator)

Anesthesiology

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Accessories to Continuous Ventilators (Respirators) are supplementary components used in conjunction with continuous ventilators to support their operation, such as breathing circuits, filters, humidifiers, and connectors. Classified as FDA Class 2 under 21 CFR 868.5895 in the Anesthesiology specialty, these accessories require 510(k) premarket notification. The product code is MOD, and these accessories are eligible for third-party 510(k) review.

510(k) Clearances

13 matches
K Number
Device Name
EveryWare
Care Cycle Connect Application
BERNOULLI MANAGEMENT SYSTEM, OXINET III AND LIFEGARD VUE
VENTLINK SYSTEM
IISIS, VERSION 1.0
AIR SAFETY HEPA, MODEL 3500
IMPACT, UNIVERSAL SINGLE-LIMB, VENTILATOR CIRCUIT, MODEL 820-0099-00
TRI-PLEX ADAPTER
BERNOULLI VENTILATOR MANAGEMENT SYSTEM
VENTNET; CENTRAL MONITORING STATION
BICORE SMARTCATH INTRATRACHEAL CATHETER
VENTILATION MECHANICS MONITOR MODEL VMM-100
NEWPORT COMMUNICAT PROTOCOL INTERFACE ADAPTOR

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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