meddevicedb.com FDA Device Reference

MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO

K873659 Class II Traditional
Decision Date
1988-04-21
Sponsor / Applicant
Universal Gym Equipment, Inc.

Technical Specification

510(k) Submission ID K873659
Product Code IKK
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1925
Decision Date 1988-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO received FDA 510(k) clearance under submission number K873659, sponsored by Universal Gym Equipment, 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 1988-04-21.

Classification & Regulation

This clearance is catalogued under FDA product code IKK and 21 CFR 890.1925, within the Physical Medicine review panel as a Class II device.