meddevicedb.com FDA Device Reference

SURGICAL DRAPES

K002419 Class II Special
Decision Date
2000-08-15
Sponsor / Applicant
Allegiance Healthcare Coporation

Technical Specification

510(k) Submission ID K002419
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2000-08-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL DRAPES received FDA 510(k) clearance under submission number K002419, sponsored by Allegiance Healthcare Coporation. 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 2000-08-15.

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.