meddevicedb.com FDA Device Reference

Technoweb Surgical Mask

K172500 Class II Traditional
Decision Date
2018-03-01
Sponsor / Applicant
Yts Global, Inc.

Technical Specification

510(k) Submission ID K172500
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2018-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Technoweb Surgical Mask received FDA 510(k) clearance under submission number K172500, sponsored by Yts Global, 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 2018-03-01.

Classification & Regulation

This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.