meddevicedb.com FDA Device Reference

MICROCOOL BREATHABLE HIGH PERFORMANCE SURGICAL GOWNS

K103406 Class II Traditional
Decision Date
2010-12-23
Sponsor / Applicant
Kimberly-Clark Corp.

Technical Specification

510(k) Submission ID K103406
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2010-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROCOOL BREATHABLE HIGH PERFORMANCE SURGICAL GOWNS received FDA 510(k) clearance under submission number K103406, sponsored by Kimberly-Clark Corp.. 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 2010-12-23.

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.