Cleared Traditional

K202285 - Medline ENfit OTC Feeding Syringe (FDA 510(k) Clearance)

Oct 2020
Decision
58d
Days
Class 2
Risk

K202285 is an FDA 510(k) clearance for the Medline ENfit OTC Feeding Syringe. This device is classified as a Enteral Syringes With Enteral Specific Connectors (Class II - Special Controls, product code PNR).

Submitted by Medline Industries, Inc. (Northfiled, US). The FDA issued a Cleared decision on October 9, 2020, 58 days after receiving the submission on August 12, 2020.

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 K202285 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 12, 2020
Decision Date October 09, 2020
Days to Decision 58 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.