meddevicedb.com FDA Device Reference

iMask Disposable Surgical Face Mask

K201182 Class II Traditional
Decision Date
2021-02-19
Sponsor / Applicant
Pac-Dent, Inc.

Technical Specification

510(k) Submission ID K201182
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

iMask Disposable Surgical Face Mask received FDA 510(k) clearance under submission number K201182, sponsored by Pac-Dent, 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 2021-02-19.

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.