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FDA 510(k)

Cyber Blade

K-Number: K192499 · 2020-07-31

ApplicantSIDAM S.r.l.
Decision Date2020-07-31
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

What is the Cyber Blade?

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

When was Cyber Blade approved by the FDA?

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

What company makes Cyber Blade?

Cyber Blade is manufactured by SIDAM S.r.l..

What is the FDA product code for Cyber Blade?

The FDA product code for Cyber Blade is GCJ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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