FDA 510(k)

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters

Número K: K230669 · 2023-11-30

Data da decisão2023-11-30

Código do produtoLJS

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Devices. It received FDA 510(k) clearance on 2023-11-30 under 510(k) number K230669. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters is a medical device that received FDA 510(k) clearance on 2023-11-30. The listed applicant is Argon Medical Devices. The 510(k) number is K230669.

When did L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters receive FDA 510(k) clearance?

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters received FDA 510(k) clearance on 2023-11-30, under 510(k) number K230669.

Who is the listed applicant for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?

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

What is the FDA product code for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?

The FDA product code for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters is LJS.

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Fonte oficial

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