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: BSS FDA class 2

Tube, Nasogastric

Gastroenterology, Urology

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The Tube, Nasogastric is a flexible tube inserted through the nose and advanced into the stomach, used for feeding, medication administration, or gastric drainage. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is BSS, regulated under 21 CFR 876.5980 in the Gastroenterology and Urology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

13 matches
K Number
Device Name
TurboSEAL Nasogastric Aspiration Tube
ENTERAL FEEDING TUBE
MOSS TUBES, INC. NASAL TUBE - MARK IV
ASPISAFE GASTRIC TUBE
GASTRIC, CATHETER, IRRIGATION & ASPIRATION
RADIUS ENTERAL FEEDING TUBE
AN-10S ANDERSEN TUBE WITH STYLET
TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FR
XEMEX ENTERAL NUTRITION CATHETER NASOGAS. TYPE A
ARGYLE POLYURETHANE SALEM SUMP TUBE
WILTEK NASAL BILIARY DRAINAGE SET
TECNOL NASO-GASTRIC TUBE HOLDER
FLEXIFLO ENTERAL PUMP SET

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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