IZLClass II
System, X-Ray, Mobile
21 CFR 892.1720 / Radiology
IZL is the FDA product code for System, X-Ray, Mobile, a class II device type, regulated under 21 CFR 892.1720. As of , FDA records hold 237 510(k) clearances under this code, the most recent dated , and 170 recalls.
Classification record
- Product code
- IZL
- Device name
- System, X-Ray, Mobile
- Regulation
- 21 CFR 892.1720
- Device class
- Class II
- Review panel
- Radiology
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 237
- Ingested recalls
- 170
Clearances, product code IZL
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1977 | 2 |
| 1978 | 12 |
| 1979 | 8 |
| 1980 | 2 |
| 1981 | 4 |
| 1983 | 2 |
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 2 |
| 1987 | 1 |
| 1988 | 3 |
| 1989 | 6 |
| 1990 | 2 |
| 1991 | 4 |
| 1992 | 3 |
| 1993 | 7 |
| 1994 | 5 |
| 1995 | 7 |
| 1997 | 5 |
| 1998 | 1 |
| 1999 | 1 |
| 2000 | 2 |
| 2001 | 3 |
| 2002 | 3 |
| 2003 | 3 |
| 2004 | 9 |
| 2005 | 4 |
| 2006 | 4 |
| 2007 | 3 |
| 2008 | 4 |
| 2009 | 3 |
| 2010 | 3 |
| 2011 | 6 |
| 2012 | 3 |
| 2014 | 7 |
| 2015 | 4 |
| 2016 | 6 |
| 2017 | 7 |
| 2018 | 8 |
| 2019 | 9 |
| 2020 | 9 |
| 2021 | 13 |
| 2022 | 16 |
| 2023 | 3 |
| 2024 | 9 |
| 2025 | 11 |
| 2026 | 5 |
Applicants with the most clearances
Product code IZL| Applicant | Clearances |
|---|---|
| Sedecal S.A. | 17 |
| Minxray Inc | 15 |
| General X-Ray, Inc. | 11 |
| GE Healthcare | 8 |
| Samsung Electronics Co., Ltd. | 8 |
| Eastman Kodak Company | 7 |
| Philips North America LLC | 7 |
| DRGEM Corporation | 6 |
| Siemens Medical Solutions USA, Inc. | 6 |
| Source-Ray, Inc. | 6 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.