meddevicedb.com FDA Device Reference

LIBERTY SPECIAL AND LIBERTY STAIRLIFTS

K896628 Class II Traditional
Decision Date
1990-01-12
Sponsor / Applicant
The Cheney Co.

Technical Specification

510(k) Submission ID K896628
Product Code ILK
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5150
Decision Date 1990-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIBERTY SPECIAL AND LIBERTY STAIRLIFTS received FDA 510(k) clearance under submission number K896628, sponsored by The Cheney Co.. 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 1990-01-12.

Classification & Regulation

This clearance is catalogued under FDA product code ILK and 21 CFR 890.5150, within the Physical Medicine review panel as a Class II device.