Cleared Traditional

Peristeen Anal Irrigation System

K140310 · Coloplast A/S · Gastroenterology & Urology
Sep 2015
Decision
573d
Days
Class 2
Risk

About This 510(k) Submission

K140310 is an FDA 510(k) clearance for the Peristeen Anal Irrigation System, a Tubes, Gastrointestinal (and Accessories) (Class II — Special Controls, product code KNT), submitted by Coloplast A/S (Minneapolis, US). The FDA issued a Cleared decision on September 3, 2015, 573 days after receiving the submission on February 7, 2014. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5980.

Submission Details

510(k) Number K140310 FDA.gov
FDA Decision Cleared SESE
Date Received February 07, 2014
Decision Date September 03, 2015
Days to Decision 573 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

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