Cleared Traditional

K142971 - AMT Bridle - Nasal Tube Retention System (FDA 510(k) Clearance)

May 2015
Decision
224d
Days
Class 2
Risk

K142971 is an FDA 510(k) clearance for the AMT Bridle - Nasal Tube Retention System. This device is classified as a Tubes, Gastrointestinal (and Accessories) (Class II - Special Controls, product code KNT).

Submitted by Applied Medical Technology, Inc. (Brecksville, US). The FDA issued a Cleared decision on May 26, 2015, 224 days after receiving the submission on October 14, 2014.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5980.

Submission Details

510(k) Number K142971 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 14, 2014
Decision Date May 26, 2015
Days to Decision 224 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code KNT — Tubes, Gastrointestinal (and Accessories)
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5980