meddevicedb.com FDA Device Reference

Puravita Medical Fold Flat Surgical Mask

K212740 Class II Traditional
Decision Date
2021-12-02
Sponsor / Applicant
Puravita M, LLC

Technical Specification

510(k) Submission ID K212740
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-12-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Puravita Medical Fold Flat Surgical Mask received FDA 510(k) clearance under submission number K212740, sponsored by Puravita M, LLC. 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 2021-12-02.

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.