Cleared Traditional

K142128 - KANGAROO ENTERAL FEEDING SYRINGES WITH ENFIT CONNECTOR (FDA 510(k) Clearance)

Feb 2015
Decision
203d
Days
Class 2
Risk

K142128 is an FDA 510(k) clearance for the KANGAROO ENTERAL FEEDING SYRINGES WITH ENFIT CONNECTOR. This device is classified as a Enteral Syringes With Enteral Specific Connectors (Class II - Special Controls, product code PNR).

Submitted by Covidien (Mansfield, US). The FDA issued a Cleared decision on February 23, 2015, 203 days after receiving the submission on August 4, 2014.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5980. Delivers Nutrition, Medication, Or Hydration Orally Or To A Gastrointestinal Tube Or Extension Set Using Aami/cn3(ps):2014 Compliant Connectors..

Submission Details

510(k) Number K142128 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 2014
Decision Date February 23, 2015
Days to Decision 203 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code PNR — Enteral Syringes With Enteral Specific Connectors
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5980
Definition Delivers Nutrition, Medication, Or Hydration Orally Or To A Gastrointestinal Tube Or Extension Set Using Aami/cn3(ps):2014 Compliant Connectors.