FACIAL SPA

Stimulator, Transcutaneous Electrical, Aesthetic Purposes

NUSKIN

The following data is part of a premarket notification filed by Nuskin with the FDA for Facial Spa.

Pre-market Notification Details

• Device ID: K122711
• 510k Number: K122711
• Device Name: FACIAL SPA
• Classification: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
• Applicant: NUSKIN ONE METRO CENTER 700 12TH STREET, SUITE 900 Washington, DC 20005
• Contact: Paul Rubin
• Correspondent: Paul Rubin; NUSKIN ONE METRO CENTER 700 12TH STREET, SUITE 900 Washington, DC 20005
• Product Code: NFO
• CFR Regulation Number: 882.5890 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2012-09-04
• Decision Date: 2013-09-17
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00860196000303	K122711	000