meddevicedb.com FDA Device Reference

nPro Surgical Mask

K203265 Class II Abbreviated
Decision Date
2021-02-09
Sponsor / Applicant
Np Medical, Inc.

Technical Specification

510(k) Submission ID K203265
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2021-02-09
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

nPro Surgical Mask received FDA 510(k) clearance under submission number K203265, sponsored by Np Medical, 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 2021-02-09.

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.