Disposable Intermittent Catheter (TPU Catheter)

FDA 510(k) K243175 · Chengdu Daxan Innovative Medical Tech. Co., Ltd.

Substantially Equivalent

510(k) numberK243175

Submission

Device name
Disposable Intermittent Catheter (TPU Catheter)
Applicant
Chengdu Daxan Innovative Medical Tech. Co., Ltd.
Chengdu, CN
Received
September 30, 2024
Decision date
June 26, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EZD – Catheter, Straight
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5130
Specialty
Gastroenterology, Urology

Other 510(k)s with product code EZD

510(k)DeviceApplicantDecision
K260737Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure…EZD · Traditional Convatec08/05/2026SE
K261658LoFric Origo Pro CoudéEZD · Special Wellspect AB07/17/2026SE
K262045Luja SoftEZD · Special Coloplast A.S.07/07/2026SE
K260394Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR)EZD · Traditional Hangzhou Jimushi Meditech Co., Ltd.06/24/2026SE
K253295Coude Sleeved IC; Coude Plus Sleeved ICEZD · Traditional Hollister Incorporated05/18/2026SE
K260999LoFric Elle ProEZD · Special Wellspect AB04/24/2026SE
K252943GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for WomenEZD · Traditional Convatec Limited04/01/2026SE
K260502Liv Pre-lubricated Intermittent CatheterEZD · Traditional HR Healthcare03/12/2026SE
K251274EZ-Protect Hydrophilic Closed System Intermittent Catheter; EZ-Protect Hydrophilic…EZD · Traditional HR Healthcare01/29/2026SESK
K251178Ready to use Nelaton CatheterEZD · Traditional Jamjoom Fullcare Corporation01/02/2026SE

More from Jamjoom Fullcare Corporation

510(k)DeviceDecision
K212567PVC Hydrophilic Urethral CatheterEZD · Traditional 12/07/2022SE

Questions and answers

When was Disposable Intermittent Catheter (TPU Catheter) cleared by the FDA?

Disposable Intermittent Catheter (TPU Catheter) (K243175) received a 510(k) decision of Substantially Equivalent on June 26, 2025, 269 days after the submission was received.

What is the product code of K243175?

The FDA product code is EZD – Catheter, Straight, a Class II (moderate risk) device regulated under 21 CFR 876.5130.