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FDA 510(k)

FACIAL SPA

K-Number: K122711 · 2013-09-17

ApplicantNuskin
Decision Date2013-09-17
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FACIAL SPA is the device name listed in this FDA 510(k) record. The listed applicant is Nuskin. It received FDA 510(k) clearance on 2013-09-17 under 510(k) number K122711. 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 FACIAL SPA?

FACIAL SPA is a medical device that received FDA 510(k) clearance on 2013-09-17. The listed applicant is Nuskin. The 510(k) number is K122711.

When did FACIAL SPA receive FDA 510(k) clearance?

FACIAL SPA received FDA 510(k) clearance on 2013-09-17, under 510(k) number K122711.

Who is the listed applicant for FACIAL SPA?

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

What is the FDA product code for FACIAL SPA?

The FDA product code for FACIAL SPA is NFO.

Related Clinical Trials

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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