meddevicedb.com FDA Device Reference

BOUNDARY SURGICAL DRAPES WITH ADHESIVE

K802652 Class II Traditional
Decision Date
1980-11-12
Sponsor / Applicant
Procter & Gamble Mfg. Co.

Technical Specification

510(k) Submission ID K802652
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1980-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOUNDARY SURGICAL DRAPES WITH ADHESIVE received FDA 510(k) clearance under submission number K802652, sponsored by Procter & Gamble Mfg. Co.. 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 1980-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.