Nutra Face Lift Model PE8050
K-Number: K150826 · 2016-02-10
ApplicantNutra Luxe MD, LLC
Decision Date2016-02-10
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Nutra Face Lift Model PE8050 is a medical device manufactured by Nutra Luxe MD, LLC. It received FDA 510(k) clearance on 2016-02-10 under approval number K150826. 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 Nutra Face Lift Model PE8050?
Nutra Face Lift Model PE8050 is a medical device that received FDA 510(k) clearance on 2016-02-10. It is manufactured by Nutra Luxe MD, LLC. The 510(k) number is K150826.
When was Nutra Face Lift Model PE8050 approved by the FDA?
Nutra Face Lift Model PE8050 received FDA 510(k) clearance on 2016-02-10, under approval number K150826.
What company makes Nutra Face Lift Model PE8050?
Nutra Face Lift Model PE8050 is manufactured by Nutra Luxe MD, LLC.
What is the FDA product code for Nutra Face Lift Model PE8050?
The FDA product code for Nutra Face Lift Model PE8050 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.