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.

Let the assistant find your predicates

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

Free to try · every answer cites its records

Product Code: LRQ FDA class 1

Tracheostomy And Nasal Suctioning Kit

Unknown

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The Tracheostomy and Nasal Suctioning Kit is a prepackaged, sterile convenience kit containing the supplies necessary to perform suctioning of tracheostomy sites or nasal passages, established in accordance with the May 20, 1997 FDA guidance on convenience kits interim regulatory guidance. It is classified as a Class 1 (lowest risk) device, subject only to general controls, representing the least burdensome regulatory category. The product code is LRQ; no specific regulation number is on file, and the medical specialty is not categorized. No special flags apply to this device.

510(k) Clearances

6 matches
K Number
Device Name
TRACHEOSTOMY KIT
MEDCARE TRACHEOSTOMY CARE TRAY
READY NURSE SYSTEM (RNS) TRACH CARE KIT
GENT-L-KARE TRACHEOSTOMY TRAYS
TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1
TRACHEOSTOMY CARE TRAY

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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