Colostomy Device W/ Pressure Lid

FDA 510(k) K790750 · Vabar Corp.

Substantially Equivalent

510(k) numberK790750

Submission

Device name
Colostomy Device W/ Pressure Lid
Applicant
Vabar Corp.
Walker, MI, US
Received
April 17, 1979
Decision date
May 14, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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
K121833Ostomy Irrigation SetEXD · Special Coloplast A/S07/16/2012SE
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
K770251Super X AdjustretteEXD · Traditional Qualitone02/28/1977SE

More from Qualitone

510(k)DeviceDecision
K790749Colostomy Enema DeviceEXD · Traditional 05/16/1979SE

Questions and answers

When was Colostomy Device W/ Pressure Lid cleared by the FDA?

Colostomy Device W/ Pressure Lid (K790750) received a 510(k) decision of Substantially Equivalent on May 14, 1979, 27 days after the submission was received.

What is the product code of K790750?

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