FDA 510(k)

Reusable Interface Cable 1.5 m (PRD-IFC-002)

N.º K: K242061 · 2024-08-15

Fecha de decisión2024-08-15

Código de productoKNS

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Reusable Interface Cable 1.5 m (PRD-IFC-002) is the device name listed in this FDA 510(k) record. The listed applicant is Creo Medical, Ltd.. It received FDA 510(k) clearance on 2024-08-15 under 510(k) number K242061. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Reusable Interface Cable 1.5 m (PRD-IFC-002)?

Reusable Interface Cable 1.5 m (PRD-IFC-002) is a medical device that received FDA 510(k) clearance on 2024-08-15. The listed applicant is Creo Medical, Ltd.. The 510(k) number is K242061.

When did Reusable Interface Cable 1.5 m (PRD-IFC-002) receive FDA 510(k) clearance?

Reusable Interface Cable 1.5 m (PRD-IFC-002) received FDA 510(k) clearance on 2024-08-15, under 510(k) number K242061.

Who is the listed applicant for Reusable Interface Cable 1.5 m (PRD-IFC-002)?

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

What is the FDA product code for Reusable Interface Cable 1.5 m (PRD-IFC-002)?

The FDA product code for Reusable Interface Cable 1.5 m (PRD-IFC-002) is KNS.

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Otros registros que enlistan a Creo Medical, Ltd. como solicitante

K242774SpydrBlade Flex Instrument (PRD-RG1-001)K242983CROMA Electrosurgical Generator (PRD-EMR-050)K230328Speedboat Flush SB1 Instrument K223138Instrumento Electrosurgical AB1, Sistema Electrosurgical Creo K221672Creo Electrosurgical System with NP1 Instrument K200298ABI Instrumento, Sistema Electrosurgical Creo

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Dispositivos relacionados (Código: KNS)

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Fuente oficial

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