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FDA 510(k)

Nutra Face Lift Model PE8050

K-Number: K150826 · 2016-02-10

Decision Date2016-02-10
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Nutra Face Lift Model PE8050 is the device name listed in this FDA 510(k) record. The listed applicant is Nutra Luxe MD, LLC. It received FDA 510(k) clearance on 2016-02-10 under 510(k) 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. The listed applicant is Nutra Luxe MD, LLC. The 510(k) number is K150826.

When did Nutra Face Lift Model PE8050 receive FDA 510(k) clearance?

Nutra Face Lift Model PE8050 received FDA 510(k) clearance on 2016-02-10, under 510(k) number K150826.

Who is the listed applicant for Nutra Face Lift Model PE8050?

The FDA 510(k) record lists Nutra Luxe MD, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nutra Face Lift Model PE8050?

The FDA product code for Nutra Face Lift Model PE8050 is NFO.

Other records listing Nutra Luxe MD, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: NFO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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