meddevicedb.com FDA Device Reference

AVD RIGHT RADIAL DRAPE

K131571 Class II Traditional
Decision Date
2014-01-31
Sponsor / Applicant
Advanced Vascular Dynamics

Technical Specification

510(k) Submission ID K131571
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2014-01-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AVD RIGHT RADIAL DRAPE received FDA 510(k) clearance under submission number K131571, sponsored by Advanced Vascular Dynamics. 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 2014-01-31.

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.