meddevicedb.com FDA Device Reference

NORTHSTAR LIDOCAINE IONTOPHORETIC CONTROLLER (NORTHSTAR CONTROLLER-D)

K031551 Class II Traditional
Decision Date
2003-08-20
Sponsor / Applicant
Vyteris, Inc.

Technical Specification

510(k) Submission ID K031551
Product Code KTB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5525
Decision Date 2003-08-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NORTHSTAR LIDOCAINE IONTOPHORETIC CONTROLLER (NORTHSTAR CONTROLLER-D) received FDA 510(k) clearance under submission number K031551, sponsored by Vyteris, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2003-08-20.

Classification & Regulation

This clearance is catalogued under FDA product code KTB and 21 CFR 890.5525, within the Physical Medicine review panel as a Class II device.