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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 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.

Frequently Asked Questions

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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Related Devices (Code: GCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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

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