meddevicedb.com FDA Device Reference

ANTI-INFECTION SHIELD

K872935 Class II Traditional
Decision Date
1987-11-09
Sponsor / Applicant
Stackhouse Assoc.

Technical Specification

510(k) Submission ID K872935
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1987-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANTI-INFECTION SHIELD received FDA 510(k) clearance under submission number K872935, sponsored by Stackhouse Assoc.. 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 1987-11-09.

Classification & Regulation

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