meddevicedb.com FDA Device Reference

CHALLENGE 6000 POWERED MUSCLE STIMULATOR

K901769 Class II Traditional
Decision Date
1990-07-03
Sponsor / Applicant
Maximum Performance Technologies, Mpts, Inc.

Technical Specification

510(k) Submission ID K901769
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1990-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHALLENGE 6000 POWERED MUSCLE STIMULATOR received FDA 510(k) clearance under submission number K901769, sponsored by Maximum Performance Technologies, Mpts, 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 1990-07-03.

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.