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FDA 510(k)

SpeedCath Compact Male

N.º K: K210250 · 2022-04-26

SolicitanteColoplast
Fecha de decisión2022-04-26
Código de productoEZD
Comité asesorGU
DecisiónSubstantially Equivalent

Resumen del dispositivo

SpeedCath Compact Male is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast. It received FDA 510(k) clearance on 2022-04-26 under 510(k) number K210250. 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 SpeedCath Compact Male?

SpeedCath Compact Male is a medical device that received FDA 510(k) clearance on 2022-04-26. The listed applicant is Coloplast. The 510(k) number is K210250.

When did SpeedCath Compact Male receive FDA 510(k) clearance?

SpeedCath Compact Male received FDA 510(k) clearance on 2022-04-26, under 510(k) number K210250.

Who is the listed applicant for SpeedCath Compact Male?

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

What is the FDA product code for SpeedCath Compact Male?

The FDA product code for SpeedCath Compact Male is EZD.

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Otros registros que enlistan a Coloplast como solicitante

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K241028Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)K231891Virtue Male Sling System with Alexis Wound Retractor Convenience KitK230165Luja 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 Coudé (20106 Male CH16 - large packaging)K223821Self-Cath Closed SystemK221401Self-Cath and Self-Cath PlusK222059SpeediCath Flex Set

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Dispositivos relacionados (Código: EZD)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K261418Liquick X-treme, Liquick X-treme PlusTeleflex MedicalK260737Cure 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).ConvatecK261658LoFric Origo Pro CoudéWellspect ABK262045Luja SoftColoplast A.S.K260394Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR)Hangzhou Jimushi Meditech Co., Ltd.K253295Coude Sleeved IC; Coude Plus Sleeved ICHollister Incorporated

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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