FDA 510(k)

Coude Sleeved IC; Coude Plus Sleeved IC

N.º K: K253295 · 2026-05-18

Fecha de decisión2026-05-18

Código de productoEZD

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Coude Sleeved IC; Coude Plus Sleeved IC is the device name listed in this FDA 510(k) record. The listed applicant is Hollister Incorporated. It received FDA 510(k) clearance on 2026-05-18 under 510(k) number K253295. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Coude Sleeved IC; Coude Plus Sleeved IC?

Coude Sleeved IC; Coude Plus Sleeved IC is a medical device that received FDA 510(k) clearance on 2026-05-18. The listed applicant is Hollister Incorporated. The 510(k) number is K253295.

When did Coude Sleeved IC; Coude Plus Sleeved IC receive FDA 510(k) clearance?

Coude Sleeved IC; Coude Plus Sleeved IC received FDA 510(k) clearance on 2026-05-18, under 510(k) number K253295.

Who is the listed applicant for Coude Sleeved IC; Coude Plus Sleeved IC?

The FDA 510(k) record lists Hollister Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Coude Sleeved IC; Coude Plus Sleeved IC?

The FDA product code for Coude Sleeved IC; Coude Plus Sleeved IC is EZD.

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Otros registros que enlistan a Hollister Incorporated como solicitante

K251468Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket (name not finalized) Sleeved IC 3 Plus (name not finalized) Sleeved IC 3 Plus Pocket (name not finalized) (N/A)K233524Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved IC 2 Plus (Name not Finalized); Sleeved IC 2 Pocket (Name not Finalized); Sleeved IC 2 Plus Pocket (Name not Finalized)K220667Sleeved IC K213575Female IC (Not Finalized)K211436Intermittent Catheter (Not Finalized)K193148VaPro Plus Pocket, VaPro Plus

Ver todos los 11 dispositivos →

Dispositivos relacionados (Código: EZD)

K261418Liquick X-treme, Liquick X-treme PlusTeleflex Medical K260737Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Straight (CH06 - CH18); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Coude (CH10 - CH18).Convatec K261658LoFric Origo Pro CoudéWellspect AB K262045Luja SoftColoplast A.S.K260394Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR)Hangzhou Jimushi Meditech Co., Ltd.K260999LoFric Elle ProWellspect AB

Fuente oficial

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