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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: SDT FDA class 2

Intra-Pulmonary Percussive Vibration (Ipv) Devices

Anesthesiology

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Intra-pulmonary percussive vibration (IPV) devices are respiratory therapy devices intended to mobilize mucus using vibration and/or pressure delivered through a mouthpiece into the airways, facilitating airway clearance in patients with conditions such as cystic fibrosis, chronic obstructive pulmonary disease, or other conditions causing mucus retention. They are classified as FDA Class II (510(k) required) under regulation 868.5665 in the Anesthesiology specialty, with product code SDT. The device is not an implant and does not support life-sustaining functions.

510(k) Clearances

3 matches
K Number
Device Name
SIMEOX 200 Airway Clearance Device
VIBRALUNG ACOUSTICAL PERCUSSOR
RESPIRONICS SIMPLYCLEAR DEVICE

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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