meddevicedb.com FDA Device Reference

MASC Surgical Mask

K211984 Class II Traditional
Decision Date
2021-07-25
Sponsor / Applicant
Mid-America Safety Corp.

Technical Specification

510(k) Submission ID K211984
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MASC Surgical Mask received FDA 510(k) clearance under submission number K211984, sponsored by Mid-America Safety 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 2021-07-25.

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.