meddevicedb.com FDA Device Reference

SURGICAL GOWN (EO STERILIZED)

K112796 Class II Traditional
Decision Date
2013-09-12
Sponsor / Applicant
Cobes Industries Co., Ltd.

Technical Specification

510(k) Submission ID K112796
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2013-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL GOWN (EO STERILIZED) received FDA 510(k) clearance under submission number K112796, sponsored by Cobes Industries 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 2013-09-12.

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.