meddevicedb.com FDA Device Reference

BC-001+ Acne Purifier

K170260 Class II Traditional
Decision Date
2017-04-25
Sponsor / Applicant
Oriental Inspiration Limited

Technical Specification

510(k) Submission ID K170260
Product Code OLP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2017-04-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BC-001+ Acne Purifier received FDA 510(k) clearance under submission number K170260, sponsored by Oriental Inspiration Limited. 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 2017-04-25.

Classification & Regulation

This clearance is catalogued under FDA product code OLP and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.