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FDA 510(k)

LILY Extension Tube and Needleless Connector

Número K: K222780 · 2023-11-09

RequerenteLily Medical Corporation
Data da decisão2023-11-09
Código do produtoFPA
Comité consultivoHO
DecisãoSubstantially Equivalent

Resumo do 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.

Perguntas frequentes

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)

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Fonte oficial

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