meddevicedb.com FDA Device Reference

MEDLINE STERILE DISPOSABLE SURGICAL GOWNS

K062969 Class II Special
Decision Date
2006-12-14
Sponsor / Applicant
Medline Industries, Inc.

Technical Specification

510(k) Submission ID K062969
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2006-12-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDLINE STERILE DISPOSABLE SURGICAL GOWNS received FDA 510(k) clearance under submission number K062969, sponsored by Medline Industries, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2006-12-14.

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.