meddevicedb.com FDA Device Reference

BARRIER SURGICAL DRAPES

K051625 Class II Special
Decision Date
2005-07-14
Sponsor / Applicant
Molnlycke Health Care, Inc.

Technical Specification

510(k) Submission ID K051625
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2005-07-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BARRIER SURGICAL DRAPES received FDA 510(k) clearance under submission number K051625, sponsored by Molnlycke Health Care, 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 2005-07-14.

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.