FRJClass I

Chair, Geriatric

21 CFR 880.6140 / General Hospital

FRJ is the FDA product code for Chair, Geriatric, a class I device type, regulated under 21 CFR 880.6140. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: FRJ
Device name: Chair, Geriatric
Regulation: 21 CFR 880.6140
Device class: Class I
Review panel: General Hospital
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: Yes
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 24 companies shown, in name order

Recent clearances

Product code FRJ

FDA records hold no clearances under product code FRJ.

Recent recalls

Product code FRJ

Z-0860-2016Class IIThe recliners were shipped without the foot rest ottoman linkage side shields, which could result in consumer injury.Hill-Rom, Inc. / initiated 2016-01-20 / 216

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)