meddevicedb.com FDA Device Reference

DISPOSABLE SURGICAL GOWNS

K120192 Class II Traditional
Decision Date
2012-10-16
Sponsor / Applicant
Weihai Hongyu Nonwoven Fabric Products Co., Ltd.

Technical Specification

510(k) Submission ID K120192
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2012-10-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE SURGICAL GOWNS received FDA 510(k) clearance under submission number K120192, sponsored by Weihai Hongyu Nonwoven Fabric Products Co., Ltd.. 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 2012-10-16.

Classification & Regulation

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