meddevicedb.com FDA Device Reference

HONGYU DISPOSABLE SURGICAL DRAPES

K141324 Class II Traditional
Decision Date
2015-04-14
Sponsor / Applicant
Weihai Hongyu Nonwoven Fabric Products Co., Ltd.

Technical Specification

510(k) Submission ID K141324
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2015-04-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HONGYU DISPOSABLE SURGICAL DRAPES received FDA 510(k) clearance under submission number K141324, 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 2015-04-14.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.