Luja Coudé (20118 Male CH8 - small packaging (Pocket size)), Luja Coudé (20111 Male CH10 - small packaging (Pocket size)), Luja Coudé (20112 Male CH12 - small packaging (Pocket size)), Luja Coudé (20114 Male CH14 - small packaging (Pocket size)), Luja Coudé (20101 Male CH10 - large packaging), Luja Coudé (20102 Male CH12 - large packaging), Luja Coudé (20104 Male CH14 - large packaging), Luja Coud

FDA 510(k) K230165 · Coloplast

Substantially Equivalent

510(k) numberK230165

Submission

Device name
Luja Coudé (20118 Male CH8 - small packaging (Pocket size)), Luja Coudé (20111 Male CH10 - small packaging (Pocket size)), Luja Coudé (20112 Male CH12 - small packaging (Pocket size)), Luja Coudé (20114 Male CH14 - small packaging (Pocket size)), Luja Coudé (20101 Male CH10 - large packaging), Luja Coudé (20102 Male CH12 - large packaging), Luja Coudé (20104 Male CH14 - large packaging), Luja Coud
Applicant
Coloplast
Plymouth, MN, US
Received
January 20, 2023
Decision date
August 25, 2023
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
K252140Heylo™ SystemEXB · Traditional 10/06/2025SE
K251116Luja CoudéEZD · Traditional 06/27/2025SE
K250270Luja SetEZD · Special 04/17/2025SE
K242049SureCath SetEZD · Traditional 11/26/2024SE
K241210Luja CoudeEZD · Traditional 11/21/2024SE
K242173Retrace Ureteral Access Sheath (ASXL10, ASXL12, ACXL10, ACXL12, AXXL10, AXXL12, ALXL10…FED · Traditional 11/12/2024SE
K242473Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551)…PAH · Traditional 10/18/2024SE
K241028Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)EZD · Traditional 07/26/2024SE
K233411Folysil Silicone CatheterEZL · Traditional 04/15/2024SE
K231953Biatain Fiber Ag (33570 - 5 cm x 5 cm / 2 in x 2 in); Biatain Fiber Ag (33572 - 10 cm x…FRO · Traditional 03/22/2024SE

Questions and answers

When was Luja Coudé (20118 Male CH8 - small packaging (Pocket size)), Luja Coudé (20111 Male CH10 - small packaging (Pocket size)), Luja Coudé (20112 Male CH12 - small packaging (Pocket size)), Luja Coudé (20114 Male CH14 - small packaging (Pocket size)), Luja Coudé (20101 Male CH10 - large packaging), Luja Coudé (20102 Male CH12 - large packaging), Luja Coudé (20104 Male CH14 - large packaging), Luja Coud cleared by the FDA?

Luja Coudé (20118 Male CH8 - small packaging (Pocket size)), Luja Coudé (20111 Male CH10 - small packaging (Pocket size)), Luja Coudé (20112 Male CH12 - small packaging (Pocket size)), Luja Coudé (20114 Male CH14 - small packaging (Pocket size)), Luja Coudé (20101 Male CH10 - large packaging), Luja Coudé (20102 Male CH12 - large packaging), Luja Coudé (20104 Male CH14 - large packaging), Luja Coud (K230165) received a 510(k) decision of Substantially Equivalent on August 25, 2023, 217 days after the submission was received.

What is the product code of K230165?

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