meddevicedb.com FDA Device Reference

SPUNGUARD FACE MASK

K823078 Class II Traditional
Decision Date
1983-01-07
Sponsor / Applicant
Kimberly-Clark Corp.

Technical Specification

510(k) Submission ID K823078
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1983-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPUNGUARD FACE MASK received FDA 510(k) clearance under submission number K823078, sponsored by Kimberly-Clark 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 1983-01-07.

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.