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OPERATING ROOM TOWELS - STERILE/NON STERILE

K863871 Class II Traditional
Decision Date
1986-10-24
Sponsor / Applicant
Med-Tex, Inc.

Technical Specification

510(k) Submission ID K863871
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1986-10-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPERATING ROOM TOWELS - STERILE/NON STERILE received FDA 510(k) clearance under submission number K863871, sponsored by Med-Tex, 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 1986-10-24.

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.