meddevicedb.com FDA Device Reference

Miria Skin Treatment System

K223871 Class II Traditional
Decision Date
2023-06-22
Sponsor / Applicant
AVAVA, Inc.

Technical Specification

510(k) Submission ID K223871
Product Code ONG
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2023-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Miria Skin Treatment System received FDA 510(k) clearance under submission number K223871, sponsored by AVAVA, 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 2023-06-22.

Classification & Regulation

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