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Kangaroo Nasogastric Feeding Tube

by Chesebrough-Pond'S U.S.A. Co. 2 variants

510(k) K810854

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK810854 Date17 Apr 1981ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
KNT
Device Class
Class II
Regulation
21 CFR Part 876.5980
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 19 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Kangaroo Nasogastric Feeding Tube is a nasogastric feeding device designed for enteral nutrition delivery via the nasal passage into the stomach. It features a weighted polyurethane construction with a slimmer, lighter tip to facilitate easier insertion and placement.

This tube is intended for single-use in clinical settings such as hospitals and outpatient care. Supplied sterile, it is classified under FDA Product Code KNT for gastroenterology and urology applications. The device holds a Traditional 510(k) clearance (K810854) as substantially equivalent, with no third-party review involved.

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Questions

AI-generated answers, 19 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the Kangaroo Nasogastric Feeding Tube intended for?

    The Kangaroo Nasogastric Feeding Tube is designed for enteral nutrition delivery via the nasal passage into the stomach, as stated in its description. It is intended for single-use in clinical settings such as hospitals and outpatient care facilities.

  • How is the Kangaroo Nasogastric Feeding Tube supplied and is it sterile?

    The device is supplied sterile, as indicated in the description. It is intended for single-use, meaning it is not designed to be reused after initial application in a clinical setting.

  • What regulatory pathway was used for the Kangaroo Nasogastric Feeding Tube?

    The device received a Traditional 510(k) clearance (K810854) as substantially equivalent, with no third-party review involved, according to the authorizations and decision details provided in the data.

  • What material and design features does the Kangaroo Nasogastric Feeding Tube have?

    The tube features a weighted polyurethane construction with a slimmer, lighter tip to facilitate easier insertion and placement through the nasal passage into the stomach, as described in the device specifications.

  • What product code and classification apply to the Kangaroo Nasogastric Feeding Tube?

    The device is classified under FDA Product Code KNT for gastroenterology and urology applications, as specified in the device data under the product_code and advisory_committee fields.