Lavaging Catheters

FDA 510(k) K822061 · American Endoscopy, Inc.

Substantially Equivalent

510(k) numberK822061

Submission

Device name
Lavaging Catheters
Applicant
American Endoscopy, Inc.
Walker, MI, US
Received
July 13, 1982
Decision date
July 20, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
OCX – Endoscopic Irrigation/Suction System
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To supply sterile water, other solutions and/or suction to endoscopes during endoscopic procedures.

Other 510(k)s with product code OCX

510(k)DeviceApplicantDecision
K251986Auxiliary Water Tube MAJ-855OCX · Traditional Olympus Medical Systems Corporation09/26/2025SE
K251997Single-Use Biopsy Valve (MAJ-1555)OCX · Traditional Olympus Medical Systems Corporation09/25/2025SE
K242586ArgoCap (200.52)OCX · Traditional Ovesco Endoscopy AG05/22/2025SE
K241704Endoscopic Water PumpOCX · Traditional Hangzhou AGS MedTech Co., Ltd.03/20/2025SE
K242357Water Container (MAJ-901); Water Container (MAJ-902)OCX · Traditional Olympus Medical Systems Corporation10/07/2024SE
K241874Aspiration Catheter (2189)OCX · Traditional Hobbs Medical, Inc.09/24/2024SE
K242134ClearCap Distal AttachmentOCX · Special Finemedix Co., Ltd.08/20/2024SE
K233442troCarWash™ SystemOCX · Traditional Biotex, Inc.05/21/2024SE
K230773Endoscopy Irrigation TubingOCX · Traditional Zhejiang Chuangxiang Medical Technology Co., Ltd.11/21/2023SE
K231471Air/Water Bottle Tubing, CO2 Source TubingOCX · Traditional Zhejiang Chuangxiang Medical Technology Co., Ltd.09/08/2023SE

More from Zhejiang Chuangxiang Medical Technology Co., Ltd.

510(k)DeviceDecision
K853274American Dilatation SystemKNQ · Traditional 10/17/1985SE
K841384Proxima 1 PH MonitorFFT · Traditional 07/19/1984SE
K833491Endo Bite BlockKTI · Traditional 04/25/1984SE
K840818Biopsy ForcepsFCL · Traditional 04/13/1984SE
K833859Tamponade Balloon CuffGCP · Traditional 01/03/1984SE
K833492Percutaneous Endoscopic GastroscopyKNT · Traditional 11/29/1983SE
K832458Automatic EndoscopeNVE · Traditional 10/20/1983SE
K821818Retrieval BalloonsKOD · Traditional 09/24/1982SE
K821819Pigtail StentsFGE · Traditional 08/20/1982SE
K822062Ball Tip Coagulating ElectrodesGEI · Traditional 08/19/1982SE

Questions and answers

When was Lavaging Catheters cleared by the FDA?

Lavaging Catheters (K822061) received a 510(k) decision of Substantially Equivalent on July 20, 1982, 7 days after the submission was received.

What is the product code of K822061?

The FDA product code is OCX – Endoscopic Irrigation/Suction System, a Class II (moderate risk) device regulated under 21 CFR 876.1500.