meddevicedb.com FDA Device Reference

VECTORSURGE 4 INTERFERENTIAL THERAPY UNIT

K993821 Class II Special
Decision Date
1999-12-09
Sponsor / Applicant
Metron Medical Australia, Pty, Ltd.

Technical Specification

510(k) Submission ID K993821
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1999-12-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VECTORSURGE 4 INTERFERENTIAL THERAPY UNIT received FDA 510(k) clearance under submission number K993821, 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 1999-12-09.

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.