Cleared Traditional

K242336 - hygh-tec Drainage II (FDA 510(k) Clearance)

Jan 2025
Decision
163d
Days
Class 2
Risk

K242336 is an FDA 510(k) clearance for the hygh-tec Drainage II. This device is classified as a Tubes, Gastrointestinal (and Accessories) (Class II - Special Controls, product code KNT).

Submitted by Amb Medtec (Waghäusel, DE). The FDA issued a Cleared decision on January 17, 2025, 163 days after receiving the submission on August 7, 2024.

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

Submission Details

510(k) Number K242336 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 07, 2024
Decision Date January 17, 2025
Days to Decision 163 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