meddevicedb.com FDA Device Reference

ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL

K822711 Class I Traditional
Decision Date
1982-11-03
Sponsor / Applicant
Parker Laboratories, Inc.

Technical Specification

510(k) Submission ID K822711
Product Code FAX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5520
Decision Date 1982-11-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANTI-MIST, ANTI-FOG EYEGLASS & DENTAL received FDA 510(k) clearance under submission number K822711, sponsored by Parker Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1982-11-03.

Classification & Regulation

This clearance is catalogued under FDA product code FAX and 21 CFR 876.5520, within the Gastroenterology, Urology review panel as a Class I device.