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FDA 510(k)

THE BUZZ FACIAL TONING SYSTEM

K-Number: K102494 · 2011-12-09

ApplicantDaka International , Ltd.
Decision Date2011-12-09
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THE BUZZ FACIAL TONING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Daka International , Ltd.. It received FDA 510(k) clearance on 2011-12-09 under 510(k) number K102494. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE BUZZ FACIAL TONING SYSTEM?

THE BUZZ FACIAL TONING SYSTEM is a medical device that received FDA 510(k) clearance on 2011-12-09. The listed applicant is Daka International , Ltd.. The 510(k) number is K102494.

When did THE BUZZ FACIAL TONING SYSTEM receive FDA 510(k) clearance?

THE BUZZ FACIAL TONING SYSTEM received FDA 510(k) clearance on 2011-12-09, under 510(k) number K102494.

Who is the listed applicant for THE BUZZ FACIAL TONING SYSTEM?

The FDA 510(k) record lists Daka International , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE BUZZ FACIAL TONING SYSTEM?

The FDA product code for THE BUZZ FACIAL TONING SYSTEM is NFO.

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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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