meddevicedb.com FDA Device Reference

Surgical Gown

K213703 Class II Traditional
Decision Date
2022-03-04
Sponsor / Applicant
Wujiang Tutaike Textiles & Finishing Co., Ltd.

Technical Specification

510(k) Submission ID K213703
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2022-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Surgical Gown received FDA 510(k) clearance under submission number K213703, sponsored by Wujiang Tutaike Textiles & Finishing 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 2022-03-04.

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.