Cleared Traditional

Vesco Medical Extension Feeding Set

K192991 · Vesco Medical, LLC · Gastroenterology & Urology
Aug 2020
Decision
283d
Days
Class 2
Risk

About This 510(k) Submission

K192991 is an FDA 510(k) clearance for the Vesco Medical Extension Feeding Set, a Gastrointestinal Tubes With Enteral Specific Connectors (Class II — Special Controls, product code PIF), submitted by Vesco Medical, LLC (Columbus, US). The FDA issued a Cleared decision on August 3, 2020, 283 days after receiving the submission on October 25, 2019. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5980.

Submission Details

510(k) Number K192991 FDA.gov
FDA Decision Cleared SESE
Date Received October 25, 2019
Decision Date August 03, 2020
Days to Decision 283 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code PIF — Gastrointestinal Tubes With Enteral Specific Connectors
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.5980
Definition To Facilitate Enteral Specific Connections.

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