Cleared Traditional

Enteral Pump Syringe

K211593 · Jiangsu Caina Medical Co.,Ltd · Gastroenterology & Urology
Sep 2021
Decision
129d
Days
Class 2
Risk

About This 510(k) Submission

K211593 is an FDA 510(k) clearance for the Enteral Pump Syringe, a Enteral Syringes With Enteral Specific Connectors (Class II — Special Controls, product code PNR), submitted by Jiangsu Caina Medical Co.,Ltd (Jiangyin, CN). The FDA issued a Cleared decision on September 30, 2021, 129 days after receiving the submission on May 24, 2021. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5980.

Submission Details

510(k) Number K211593 FDA.gov
FDA Decision Cleared SESE
Date Received May 24, 2021
Decision Date September 30, 2021
Days to Decision 129 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.

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