Ostomy Irrigation Set

FDA 510(k) K121833 · Coloplast A/S

Substantially Equivalent

510(k) numberK121833

Submission

Device name
Ostomy Irrigation Set
Applicant
Coloplast A/S
Plymouth, MN, US
Received
June 22, 2012
Decision date
July 16, 2012
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EXD – Irrigator, Ostomy
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5895
Specialty
Gastroenterology, Urology

Other 510(k)s with product code EXD

510(k)DeviceApplicantDecision
K914692Urinary Diversion Evacuating CatheterEXD · Traditional Cook Urological, Inc.07/02/1992SE
K904586Palex Irrigation SetEXD · Traditional Palex Intl. SA12/28/1990SE
K871791Bloxom IrrigatorEXD · Traditional I.B. Bloxom C/O Hogan & Hartson05/20/1987SE
K840268Irrigation SystemEXD · Traditional Coloplast A/S04/05/1984SE
K832299Visi-Flow IrrigatorEXD · Traditional Convatec, A Division of E.R. Squibb & Sons08/26/1983SE
K823274Uni-Tip Colostomy Irrigation ConeEXD · Traditional Howmedica Corp.12/07/1982SE
K811160Sur-Fit Irrigation SleeveEXD · Traditional E. R. Squibb & Sons, Inc.06/02/1981SE
K790749Colostomy Enema DeviceEXD · Traditional Vabar Corp.05/16/1979SE
K790750Colostomy Device W/ Pressure LidEXD · Traditional Vabar Corp.05/14/1979SE
K770251Super X AdjustretteEXD · Traditional Qualitone02/28/1977SE

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Questions and answers

When was Ostomy Irrigation Set cleared by the FDA?

Ostomy Irrigation Set (K121833) received a 510(k) decision of Substantially Equivalent on July 16, 2012, 24 days after the submission was received.

What is the product code of K121833?

The FDA product code is EXD – Irrigator, Ostomy, a Class II (moderate risk) device regulated under 21 CFR 876.5895.