510(k) · Cleared

Cleared

Digital Radiography Cxdi-50C

K060433510(k) TraditionalCleared Mar 10, 200617-day reviewClass II21 CFR 892.1680

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Canon, Inc. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Mar 10, 2006 as substantially equivalent to K031447 (Canon, Inc., 2003) and 1 other predicate after a 17-day review. Its family tree reaches back 4 generations to 1998. 136 later devices descend from it.

Decided: Mar 10, 2006
Review: 17 days
Class: Class II
Product code: MQB
Recalls: None
Predicates: 2

Its longest line of descent runs back 4 generations to K981556 (1998). 6 ancestors in all. 136 later devices descend from it, 5 citing it directly.

By dateBy generation

Root · 4 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
3 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
2 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
1 generation backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
This deviceK060433 Digital Radiography Cxdi-50CCanon, Inc. · 2006
Descendant · cites it directly · 82 of its ownK091545 Digital Radiography Cxdi-60CCanon, Inc. · 2009
Descendant · 2 generations on · 80 of its ownK102012 Digital RadiographyCanon Inc. -Medical Equipment Group · 2010 · Recalled
Descendant · 3 generations on · 54 of its ownK103596 Wireless/Wired FDR D-Evo Flat Panel DetectorFujifilm Medical Systems U.S.A, Inc. · 2011
Descendant · 3 generations on · 52 of its ownK111548 Wireless/Wired FDR D-Evo Flat Pancel Detector System Model DR-ID600…Fujifilm Medical System U.S.A., Inc. · 2011
Descendant · 4 generations on · 50 of its ownK132509 FDR D-Evo Flat Panel Detector SystemFujifilm Medical Systems U.S.A, Inc. · 2013

Showing 5 of 136 descendants. See all descendants

Descendants cleared per year

2009high 15 (2022) · low 4 (2009)2026

Most influential descendants

Showing 5 of 136 · See all

K091545Digital Radiography Cxdi-60CCanon, Inc. · 2009 · cites it directly82descendants
K102012Digital RadiographyCanon Inc. -Medical Equipment Group · 2010 · 2 generations on80descendants
K103596Wireless/Wired FDR D-Evo Flat Panel DetectorFujifilm Medical Systems U.S.A, Inc. · 2011 · 3 generations on54descendants
K111548Wireless/Wired FDR D-Evo Flat Pancel Detector System Model DR-ID600 W/DR-ID611SEFujifilm Medical System U.S.A., Inc. · 2011 · 3 generations on52descendants
K132509FDR D-Evo Flat Panel Detector SystemFujifilm Medical Systems U.S.A, Inc. · 2013 · 4 generations on50descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−4	K981556	Canon X-Ray Digital Camera Cxdi-11	Canon USA, Inc.	1998	—
−3	K992547	Canon X-Ray Digital Camera, Model Cxdi-22	Canon USA, Inc.	1999	—
−2	K023750	Cannon Digital Radiography Model Cxdi-40G	Canon USA, Inc.	2002	—
−1	K031447	Canon, Digital Radiography, Model Cxdi-50G	Canon, Inc.	2003	—
0 (this device)	K060433	Digital Radiography Cxdi-50C	Canon, Inc.	2006	—
+1	K091545	Digital Radiography Cxdi-60C	Canon, Inc.	2009	—
+2	K102012	Digital Radiography	Canon Inc. -Medical Equipment Group	2010	1
+3	K103596	Wireless/Wired FDR D-Evo Flat Panel Detector	Fujifilm Medical Systems U.S.A, Inc.	2011	—
+3	K111548	Wireless/Wired FDR D-Evo Flat Pancel Detector System Model DR-ID600 W/DR-ID611SE	Fujifilm Medical System U.S.A., Inc.	2011	—
+4	K132509	FDR D-Evo Flat Panel Detector System	Fujifilm Medical Systems U.S.A, Inc.	2013	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
2002	1	0
2003	1	0

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2009	4	0
2010	6	0
2011	7	0
2012	4	0
2013	4	0
2014	6	0
2015	5	0
2016	8	0
2017	10	0
2018	10	0
2019	11	0
2020	7	0
2021	7	0
2022	15	0
2023	6	0
2024	10	0
2025	10	0
2026	6	0

FIG. 1 — Lineage of K060433, 1998–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in MQB? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new MQB device

#1 K201528 Yushan X-Ray Flat Panel Detector with DROCscore 21.5 · 12 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

Type	Number	Device	Applicant	Decided	Recalls
*	K031447	Canon, Digital Radiography, Model Cxdi-50G Summary page 1 …To be assigned Predicate Device: Manufacturer: Canon Inc. ‘I'ade Name: Canon Model Name: CXDI-50G Classification Name: 90MQB, Solid State X-ray Imager FDA 510(k) #: K031447 Manufacturer: Canon Inc. ‘I'ade Name: Canon Model Name: CXDI-40C Classification Name: YOMQB, Solid State X-ray lmager DA 510(…	Canon, Inc.	2003	—
*	K031633	Canon Inc., Digital Radiography, Model Cxdi-40C Summary page 1 …X-ray Imager FDA 510(k) #: K031447 Manufacturer: Canon Inc. ‘I'ade Name: Canon Model Name: CXDI-40C Classification Name: YOMQB, Solid State X-ray lmager DA 510(k) #: K031633 Description Of Device: The Canon digital radiography CX1)1-50C is used to directly capture and convert conventional projection X…	Canon USA, Inc.	2003	—

Also cleared against K031447: 15 other devices →

What descends from it? (136)

See all 136

5 later devices cite it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K091545	Digital Radiography Cxdi-60C	Canon, Inc.	2009	82
K090238	Sedecal X-Plus LP Plus Digital Diagnostic X-Ray Systems	Sedecal., Sa.	2009	46
K092439	Canon Digital Fluoroscopy and Radiography, Model Cxdi-50RF	Virtual Imaging, Inc.	2009	10
K093688	Canon, Model Urs-50RF	Virtual Imaging, Inc.	2010	5
K091436	Digital Radiography, Model Cxdi-55C	Canon, Inc.	2009	4

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

The line of descent spans 8 years and passes through 2 companies; a new generation was cleared every 2.8 years on median.
None of the 6 ancestors has a recall.
Of its descendants, K091545 (Canon, Inc., 2009) has gone furthest, with 82 descendants of its own.
15 other devices also cite its predicate K031447.

How does its category compare?

All MQB devices

MQB Solid State X-Ray Imager (Flat Panel/Digital Imager): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MQB

8in 2025

2007high 32 (2014) · low 8 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQB

127in 2025

2007high 245 (2026) · low 15 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MQB

1in 2025

2007high 36 (2008) · low 0 (2014)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MQB

141in 2025

2007high 267 (2012) · low 9 (2020)2025

MAUDE reports naming product code MQB, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	13	22	15	25
2008	8	15	36	30
2009	15	57	19	34
2010	11	116	14	39
2011	24	102	10	101
2012	22	80	8	267
2013	21	105	6	159
2014	32	102	0	29
2015	21	81	0	21
2016	22	92	0	26
2017	31	30	1	20
2018	16	30	4	84
2019	22	30	1	45
2020	19	28	4	9
2021	21	48	1	26
2022	31	48	0	13
2023	10	30	0	51
2024	8	187	0	91
2025	8	127	1	141
2026	3	245	1	—

What is it indicated for?

DIGITAL RADIOGRAPHY CXDI-50C provides digital Image capture for conventionat fim/screen radiographic examinations. The device is intended to replace radiographic film/screen systems in alt general purpose diagnostic procedures. This device is not intended for mammography applications.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

https://510kreport.com/device/K060433 · printed Nov 6, 2026

Cite this page

510(k) Report. “K060433: Digital Radiography Cxdi-50C.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K060433

Report an extraction error

Are you the manufacturer?

Record history

FDA decision record loaded May 2, 2026
Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026