meddevicedb.com FDA Device Reference

Sovereign America Surgical Face Mask

K201095 Class II Abbreviated
Decision Date
2021-03-19
Sponsor / Applicant
Homtex, Inc.

Technical Specification

510(k) Submission ID K201095
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-03-19
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sovereign America Surgical Face Mask received FDA 510(k) clearance under submission number K201095, sponsored by Homtex, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2021-03-19.

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.