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ARRIRM SCRUB BRUSH/SPONGE

K823173 Class I Traditional
Decision Date
1982-11-22
Sponsor / Applicant
The Buckeye Cellulose Corp.

Technical Specification

510(k) Submission ID K823173
Product Code GEC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1982-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARRIRM SCRUB BRUSH/SPONGE received FDA 510(k) clearance under submission number K823173, sponsored by The Buckeye Cellulose Corp.. 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 1982-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code GEC and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.