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MODIFICATION TO: COMPEL SURGICAL DRAPES

K012807 Class II Special
Decision Date
2001-10-11
Sponsor / Applicant
Standard Textile Co., Inc.

Technical Specification

510(k) Submission ID K012807
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2001-10-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO: COMPEL SURGICAL DRAPES received FDA 510(k) clearance under submission number K012807, sponsored by Standard Textile Co., Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2001-10-11.

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.