meddevicedb.com FDA Device Reference

CLOTHINGUARD

K894760 Class I Traditional
Decision Date
1989-08-18
Sponsor / Applicant
Barrier Concepts, Inc.

Technical Specification

510(k) Submission ID K894760
Product Code FYE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1989-08-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLOTHINGUARD received FDA 510(k) clearance under submission number K894760, sponsored by Barrier Concepts, 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 1989-08-18.

Classification & Regulation

This clearance is catalogued under FDA product code FYE and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class I device.