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FDA 510(k)

LILY Extension Tube and Needleless Connector

N.º K: K222780 · 2023-11-09

SolicitanteLily Medical Corporation
Fecha de decisión2023-11-09
Código de productoFPA
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

LILY Extension Tube and Needleless Connector is the device name listed in this FDA 510(k) record. The listed applicant is Lily Medical Corporation. It received FDA 510(k) clearance on 2023-11-09 under 510(k) number K222780. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the LILY Extension Tube and Needleless Connector?

LILY Extension Tube and Needleless Connector is a medical device that received FDA 510(k) clearance on 2023-11-09. The listed applicant is Lily Medical Corporation. The 510(k) number is K222780.

When did LILY Extension Tube and Needleless Connector receive FDA 510(k) clearance?

LILY Extension Tube and Needleless Connector received FDA 510(k) clearance on 2023-11-09, under 510(k) number K222780.

Who is the listed applicant for LILY Extension Tube and Needleless Connector?

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

What is the FDA product code for LILY Extension Tube and Needleless Connector?

The FDA product code for LILY Extension Tube and Needleless Connector is FPA.

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Dispositivos relacionados (Código: FPA)

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.

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Fuente oficial

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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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