meddevicedb.com FDA Device Reference

DISPOSABLE MEDICAL GOWNS

K891820 Class II Traditional
Decision Date
1989-07-24
Sponsor / Applicant
Bioshield, Inc.

Technical Specification

510(k) Submission ID K891820
Product Code FYB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1989-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE MEDICAL GOWNS received FDA 510(k) clearance under submission number K891820, sponsored by Bioshield, 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 1989-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code FYB and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.