meddevicedb.com FDA Device Reference

PREVENTION BREATHABLE, IMPERVIOUS SURGICAL GOWNS

K043017 Class II Traditional
Decision Date
2005-03-08
Sponsor / Applicant
Medline Industries, Inc.

Technical Specification

510(k) Submission ID K043017
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2005-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREVENTION BREATHABLE, IMPERVIOUS SURGICAL GOWNS received FDA 510(k) clearance under submission number K043017, sponsored by Medline Industries, Inc.. 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 2005-03-08.

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.