FDA 510(k)

da Vinci E-200 Electrosurgical Generator

N.º K: K223039 · 2022-11-28

Fecha de decisión2022-11-28

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

da Vinci E-200 Electrosurgical Generator is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Surgical. It received FDA 510(k) clearance on 2022-11-28 under 510(k) number K223039. 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 da Vinci E-200 Electrosurgical Generator?

da Vinci E-200 Electrosurgical Generator is a medical device that received FDA 510(k) clearance on 2022-11-28. The listed applicant is Intuitive Surgical. The 510(k) number is K223039.

When did da Vinci E-200 Electrosurgical Generator receive FDA 510(k) clearance?

da Vinci E-200 Electrosurgical Generator received FDA 510(k) clearance on 2022-11-28, under 510(k) number K223039.

Who is the listed applicant for da Vinci E-200 Electrosurgical Generator?

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

What is the FDA product code for da Vinci E-200 Electrosurgical Generator?

The FDA product code for da Vinci E-200 Electrosurgical Generator is GEI.

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Otros registros que enlistan a Intuitive Surgical como solicitante

K260695da Vinci Firefly Imaging System K241635da Vinci E-200 Electrosurgical Generator K241621Da Vinci Monopolar and Bipolar Adapters (378896)K240723da Vinci Xi Surgical System (IS4000); da Vinci X Surgical System (IS4200)K231212da Vinci E-200 Electrosurgical Generator K192803da Vinci Xi Surgical System, da Vinci X Surgical System

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Fuente oficial

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