meddevicedb.com FDA Device Reference

SUMMIT STAIRWAY LIFT

K032880 Class II Abbreviated
Decision Date
2003-11-10
Sponsor / Applicant
Summit Lifts, Inc.

Technical Specification

510(k) Submission ID K032880
Product Code ILK
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5150
Decision Date 2003-11-10
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUMMIT STAIRWAY LIFT received FDA 510(k) clearance under submission number K032880, sponsored by Summit Lifts, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2003-11-10.

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.