FDA 510(k)

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

N.º K: K230669 · 2023-11-30

Fecha de decisión2023-11-30

Código de productoLJS

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del 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.

Preguntas frecuentes

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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Otros registros que enlistan a Argon Medical Devices como solicitante

K230631Kodiak™ Dual Port Coaxial Introducer Kit K213232NovaCore Semi-Automatic Biopsy Instrument K213638Traveler 0.038 Stylet Portal Vein Access (TPS001), Traveler 21ga Needle Portal Vein Access Set (TPS002), Traveler 16ga Needle Portal Vein Access Set (TPS003)K213002SCORPION Portal Vein Access Set

Dispositivos relacionados (Código: LJS)

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Fuente oficial

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