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ENDICOTT & BEAMAN SUPRA-TEC FACE MASK

K881372 Class II Traditional
Decision Date
1988-04-08
Sponsor / Applicant
Endicott & Beaman, Inc.

Technical Specification

510(k) Submission ID K881372
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1988-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDICOTT & BEAMAN SUPRA-TEC FACE MASK received FDA 510(k) clearance under submission number K881372, sponsored by Endicott & Beaman, 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 1988-04-08.

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.