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MEDSURG STERILE O.R. TOWELS

K940175 Class II Traditional
Decision Date
1994-05-26
Sponsor / Applicant
Medsurg Industries, Inc.

Technical Specification

510(k) Submission ID K940175
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1994-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDSURG STERILE O.R. TOWELS received FDA 510(k) clearance under submission number K940175, sponsored by Medsurg Industries, 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 1994-05-26.

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.