DXJClass II

Display, Cathode-Ray Tube, Medical

21 CFR 870.2450 / Cardiovascular

DXJ is the FDA product code for Display, Cathode-Ray Tube, Medical, a class II device type, regulated under 21 CFR 870.2450. As of 2026-09-10, FDA records hold 78 510(k) clearances under this code, the most recent dated 2021-11-10, and 21 recalls.

Classification record

Product code: DXJ
Device name: Display, Cathode-Ray Tube, Medical
Regulation: 21 CFR 870.2450
Device class: Class II
Review panel: Cardiovascular
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 78
Ingested recalls: 21

Clearances, product code DXJ

By decision year

78 clearances under product code DXJ with a decision year between 1976 and 2021, 1981 the highest year at 5.

Show the numbers

510(k) clearances under FDA product code DXJ by decision year
Year	Clearances
1976	2
1977	1
1978	3
1980	1
1981	5
1982	2
1983	5
1984	2
1985	5
1986	1
1987	1
1988	2
1989	2
1990	3
1991	1
1993	3
1994	2
1995	1
1997	2
1999	1
2000	1
2002	1
2006	1
2007	1
2008	1
2010	2
2011	4
2012	1
2013	3
2014	4
2015	2
2016	1
2017	4
2018	4
2020	1
2021	2

Applicants with the most clearances

Product code DXJ

Applicants holding the most 510(k) clearances under product code DXJ
Applicant	Clearances
Hewlett-Packard Co.	7
Barco N.V.	5
Litton Medical Electronics	5
Vidco, Inc.	5
Honeywell, Inc.	4
Marquette Electronics, Inc.	3
Nihon Kohden America Inc	3
Philips Medizin Systeme Boeblingen GmbH	3
Quinton, Inc.	3
LivaNova Deutschland GmbH	3

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 31 companies shown, in name order