meddevicedb.com FDA Device Reference

Carewear Firefly Wrinkle Reduction

K202442 Class II Traditional
Decision Date
2020-11-19
Sponsor / Applicant
Carewear Corp.

Technical Specification

510(k) Submission ID K202442
Product Code OHS
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2020-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Carewear Firefly Wrinkle Reduction received FDA 510(k) clearance under submission number K202442, sponsored by Carewear Corp.. 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 2020-11-19.

Classification & Regulation

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