meddevicedb.com FDA Device Reference

VX-400 TOPICAL HYPERBARIC OXYGEN CHAMBER

K022028 Class II Traditional
Decision Date
2002-12-17
Sponsor / Applicant
Vascular One, Inc.

Technical Specification

510(k) Submission ID K022028
Product Code KPJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5650
Decision Date 2002-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VX-400 TOPICAL HYPERBARIC OXYGEN CHAMBER received FDA 510(k) clearance under submission number K022028, sponsored by Vascular One, Inc.. 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 2002-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code KPJ and 21 CFR 878.5650, within the General, Plastic Surgery review panel as a Class II device.