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FDA 510(k)

FACEMASTER FACIAL TONING SYSTEM

K-Number: K040871 · 2005-06-01

ApplicantFacemaster of Beverly Hills, Inc.
Decision Date2005-06-01
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FACEMASTER FACIAL TONING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Facemaster of Beverly Hills, Inc.. It received FDA 510(k) clearance on 2005-06-01 under 510(k) number K040871. 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 FACEMASTER FACIAL TONING SYSTEM?

FACEMASTER FACIAL TONING SYSTEM is a medical device that received FDA 510(k) clearance on 2005-06-01. The listed applicant is Facemaster of Beverly Hills, Inc.. The 510(k) number is K040871.

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

FACEMASTER FACIAL TONING SYSTEM received FDA 510(k) clearance on 2005-06-01, under 510(k) number K040871.

Who is the listed applicant for FACEMASTER FACIAL TONING SYSTEM?

The FDA 510(k) record lists Facemaster of Beverly Hills, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FACEMASTER FACIAL TONING SYSTEM?

The FDA product code for FACEMASTER 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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