meddevicedb.com FDA Device Reference

MULTIMODE(TM) POWER MODULE SYSTEM

K881463 Class II Traditional
Decision Date
1988-07-18
Sponsor / Applicant
Dufco Electronics, Inc.

Technical Specification

510(k) Submission ID K881463
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 1988-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIMODE(TM) POWER MODULE SYSTEM received FDA 510(k) clearance under submission number K881463, sponsored by Dufco Electronics, 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 1988-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.