Clearance Summary
ULTRA TAN PURPLE PRO received FDA 510(k) clearance under submission number K875190, sponsored by Ultra Tan Intl. AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1988-01-14.
- Submission: K875190
- Applicant / Sponsor: Ultra Tan Intl. AB
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4635
- Decision date: 1988-01-14
Classification & Regulation
This clearance is catalogued under FDA product code LEJ and 21 CFR 878.4635, within the General, Plastic Surgery review panel as a Class II device.