FDA 510(k)

RF Cannula

N.º K: K241367 · 2025-01-23

SolicitanteShanghai Samedical & Plastic Instruments Co., Ltd.

Fecha de decisión2025-01-23

Código de productoGXI

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

RF Cannula is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Samedical & Plastic Instruments Co., Ltd.. It received FDA 510(k) clearance on 2025-01-23 under 510(k) number K241367. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the RF Cannula?

RF Cannula is a medical device that received FDA 510(k) clearance on 2025-01-23. The listed applicant is Shanghai Samedical & Plastic Instruments Co., Ltd.. The 510(k) number is K241367.

When did RF Cannula receive FDA 510(k) clearance?

RF Cannula received FDA 510(k) clearance on 2025-01-23, under 510(k) number K241367.

Who is the listed applicant for RF Cannula?

The FDA 510(k) record lists Shanghai Samedical & Plastic Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RF Cannula?

The FDA product code for RF Cannula is GXI.

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Fuente oficial

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