IXWClass II

Processor, Radiographic-Film, Automatic

21 CFR 892.1900 / Radiology

IXW is the FDA product code for Processor, Radiographic-Film, Automatic, a class II device type, regulated under 21 CFR 892.1900. As of 2026-09-10, FDA records hold 83 510(k) clearances under this code, the most recent dated 2011-08-18, and one recall.

Classification record

Product code: IXW
Device name: Processor, Radiographic-Film, Automatic
Regulation: 21 CFR 892.1900
Device class: Class II
Review panel: Radiology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 83
Ingested recalls: 1

Clearances, product code IXW

By decision year

83 clearances under product code IXW with a decision year between 1976 and 2011, 1993 the highest year at 13.

Show the numbers

510(k) clearances under FDA product code IXW by decision year
Year	Clearances
1976	1
1977	1
1978	2
1979	1
1980	1
1981	1
1983	1
1986	5
1988	7
1989	1
1990	4
1991	7
1992	6
1993	13
1994	4
1995	9
1996	2
1997	2
1998	1
1999	3
2000	3
2002	1
2003	4
2009	1
2010	1
2011	1

Applicants with the most clearances

Product code IXW

Applicants holding the most 510(k) clearances under product code IXW
Applicant	Clearances
Eastman Kodak Company	31
Konica Medical Corp.	7
Alphatek Corp.	5
FUJIFILM Healthcare Americas Corporation	4
3M Company	3
All-Pro Imaging Corp.	3
E.I. Dupont de Nemours & Co., Inc.	2
Fischer Industries, Inc.	2
JPI Healthcare Co., Ltd	2
Protec GmbH & Co. KG	2

Companies listing this code with FDA

Companies whose registered establishments list this code