FDA 510(k)

Cyber Blade

Número K: K192499 · 2020-07-31

Data da decisão2020-07-31

Código do produtoGCJ

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Cyber Blade is the device name listed in this FDA 510(k) record. The listed applicant is SIDAM S.r.l.. It received FDA 510(k) clearance on 2020-07-31 under 510(k) number K192499. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Cyber Blade?

Cyber Blade is a medical device that received FDA 510(k) clearance on 2020-07-31. The listed applicant is SIDAM S.r.l.. The 510(k) number is K192499.

When did Cyber Blade receive FDA 510(k) clearance?

Cyber Blade received FDA 510(k) clearance on 2020-07-31, under 510(k) number K192499.

Who is the listed applicant for Cyber Blade?

The FDA 510(k) record lists SIDAM S.r.l. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cyber Blade?

The FDA product code for Cyber Blade is GCJ.

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