meddevicedb.com FDA Device Reference

SNA-001 Silver Photoparticle Topical Gel

K192620 Class II Traditional
Decision Date
2020-08-12
Sponsor / Applicant
Sienna Biopharmaceuticals, Inc.

Technical Specification

510(k) Submission ID K192620
Product Code QCY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2020-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SNA-001 Silver Photoparticle Topical Gel received FDA 510(k) clearance under submission number K192620, sponsored by Sienna Biopharmaceuticals, Inc.. 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 2020-08-12.

Classification & Regulation

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