meddevicedb.com FDA Device Reference

BARRIER SURGICAL GOWNS

K990395 Class II Traditional
Decision Date
1999-04-13
Sponsor / Applicant
Johnson & Johnson Medical, Div. of Ethicon, Inc.

Technical Specification

510(k) Submission ID K990395
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1999-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BARRIER SURGICAL GOWNS received FDA 510(k) clearance under submission number K990395, sponsored by Johnson & Johnson Medical, Div. of Ethicon, 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 1999-04-13.

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.