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FDA 510(k)

AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM

K-Number: K120511 · 2012-07-30

ApplicantLeto Enterprise , Ltd.
Decision Date2012-07-30
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Leto Enterprise , Ltd.. It received FDA 510(k) clearance on 2012-07-30 under 510(k) number K120511. 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 AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM?

AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM is a medical device that received FDA 510(k) clearance on 2012-07-30. The listed applicant is Leto Enterprise , Ltd.. The 510(k) number is K120511.

When did AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM receive FDA 510(k) clearance?

AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM received FDA 510(k) clearance on 2012-07-30, under 510(k) number K120511.

Who is the listed applicant for AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM?

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

What is the FDA product code for AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM?

The FDA product code for AGELESS WONDER FACIAL MUSCLE STIMULATION 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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