meddevicedb.com FDA Device Reference

MUSCLE STIM. DEVICES, BM 2000,4000,6000,8000

K874232 Class II Traditional
Decision Date
1989-03-10
Sponsor / Applicant
Health Systems Intl., Inc.

Technical Specification

510(k) Submission ID K874232
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1989-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MUSCLE STIM. DEVICES, BM 2000,4000,6000,8000 received FDA 510(k) clearance under submission number K874232, sponsored by Health Systems Intl., 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 1989-03-10.

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.