meddevicedb.com FDA Device Reference

STERILE FILM DRAPE FENESTRATED W/ADHESIVE PATCH

K850326 Class II Traditional
Decision Date
1985-02-26
Sponsor / Applicant
Excel Health Care Products

Technical Specification

510(k) Submission ID K850326
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1985-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE FILM DRAPE FENESTRATED W/ADHESIVE PATCH received FDA 510(k) clearance under submission number K850326, sponsored by Excel Health Care Products. 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 1985-02-26.

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.