FDA 510(k)

Cross Vascular RF Generator and Footswitch (optional accessory)

N.º K: K232809 · 2023-10-12

Fecha de decisión2023-10-12

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Cross Vascular RF Generator and Footswitch (optional accessory) is the device name listed in this FDA 510(k) record. The listed applicant is Cross Vascular, Inc.. It received FDA 510(k) clearance on 2023-10-12 under 510(k) number K232809. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Cross Vascular RF Generator and Footswitch (optional accessory)?

Cross Vascular RF Generator and Footswitch (optional accessory) is a medical device that received FDA 510(k) clearance on 2023-10-12. The listed applicant is Cross Vascular, Inc.. The 510(k) number is K232809.

When did Cross Vascular RF Generator and Footswitch (optional accessory) receive FDA 510(k) clearance?

Cross Vascular RF Generator and Footswitch (optional accessory) received FDA 510(k) clearance on 2023-10-12, under 510(k) number K232809.

Who is the listed applicant for Cross Vascular RF Generator and Footswitch (optional accessory)?

The FDA 510(k) record lists Cross Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cross Vascular RF Generator and Footswitch (optional accessory)?

The FDA product code for Cross Vascular RF Generator and Footswitch (optional accessory) is GEI.

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Otros registros que enlistan a Cross Vascular, Inc. como solicitante

K232852Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable

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Fuente oficial

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