meddevicedb.com FDA Device Reference

WALL GRAB BARS 98130-98136

K842650 Class I Traditional
Decision Date
1984-08-10
Sponsor / Applicant
Guardian Products Co., Inc.

Technical Specification

510(k) Submission ID K842650
Product Code IKX
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5050
Decision Date 1984-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WALL GRAB BARS 98130-98136 received FDA 510(k) clearance under submission number K842650, sponsored by Guardian Products Co., 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 1984-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code IKX and 21 CFR 890.5050, within the Physical Medicine review panel as a Class I device.