FDA 510(k)

SpeedCath Compact Male

Número K: K210250 · 2022-04-26

Data da decisão2022-04-26

Código do produtoEZD

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do 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.

Perguntas frequentes

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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Outros registros que listam Coloplast como candidato(a)

K241028Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)K231891Virtue Male Sling System with Alexis Wound Retractor Convenience Kit K230165Luja 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 System K221401Self-Cath and Self-Cath Plus K222059SpeediCath Flex Set

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Fonte oficial

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