NuBODY Skin Toning Device
K-Number: K171588 · 2017-07-31
ApplicantCarol Cole Company Dba Nuface
Decision Date2017-07-31
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
NuBODY Skin Toning Device is a medical device manufactured by Carol Cole Company Dba Nuface. It received FDA 510(k) clearance on 2017-07-31 under approval number K171588. 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 NuBODY Skin Toning Device?
NuBODY Skin Toning Device is a medical device that received FDA 510(k) clearance on 2017-07-31. It is manufactured by Carol Cole Company Dba Nuface. The 510(k) number is K171588.
When was NuBODY Skin Toning Device approved by the FDA?
NuBODY Skin Toning Device received FDA 510(k) clearance on 2017-07-31, under approval number K171588.
What company makes NuBODY Skin Toning Device?
NuBODY Skin Toning Device is manufactured by Carol Cole Company Dba Nuface.
What is the FDA product code for NuBODY Skin Toning Device?
The FDA product code for NuBODY Skin Toning Device is NFO.
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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.