Skip to content

Hollister Nasogastric Tube Attachment Device

by Hollister, Inc.

510(k) K953232

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 NumberK953232 Date18 Aug 1995ClearedStatusActive

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  • Withdrawn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 Hollister Nasogastric Tube Attachment Device is a Feeding Tube Attachment Device (FTAD) designed to secure nasogastric tubes without tape. It provides an alternative to traditional adhesive methods, reducing skin irritation and improving patient comfort by maintaining stable tube positioning.

This device is intended for single-use in clinical settings, including gastroenterology and urology. It features an adjustable clamping mechanism for secure tube attachment and a skin barrier to protect surrounding tissue. Supplied sterile, it requires no additional regulatory approval beyond its FDA 510(k) clearance (K953232).

Other devices from Hollister, Inc.

See all devices from Hollister, Inc. →