meddevicedb.com FDA Device Reference

GERSON ISOLAIR APR PARTICULATE SURGICAL MASK

K922507 Class II Traditional
Decision Date
1992-11-16
Sponsor / Applicant
Louis M. Gerson Co., Inc.

Technical Specification

510(k) Submission ID K922507
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1992-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GERSON ISOLAIR APR PARTICULATE SURGICAL MASK received FDA 510(k) clearance under submission number K922507, sponsored by Louis M. Gerson Co., 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 1992-11-16.

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.