meddevicedb.com FDA Device Reference

FLUID RESISTANT MASK WITH WRAP AROUND EYE SHIELD

K934974 Class II Traditional
Decision Date
1994-04-13
Sponsor / Applicant
Mid America Medical, Inc.

Technical Specification

510(k) Submission ID K934974
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1994-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLUID RESISTANT MASK WITH WRAP AROUND EYE SHIELD received FDA 510(k) clearance under submission number K934974, sponsored by Mid America Medical, 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 1994-04-13.

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.