meddevicedb.com FDA Device Reference

VECTORSURGE 5 MODEL 470

K030648 Class II Special
Decision Date
2003-03-28
Sponsor / Applicant
Metron Medical Australia, Pty, Ltd.

Technical Specification

510(k) Submission ID K030648
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2003-03-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VECTORSURGE 5 MODEL 470 received FDA 510(k) clearance under submission number K030648, sponsored by Metron Medical Australia, Pty, Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2003-03-28.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.