510(k) Report

510(k) · Cleared

Cleared

EVS 4343

K142475510(k) TraditionalCleared Jan 15, 2015134-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

DRTECH Corporation · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Jan 15, 2015 as substantially equivalent to K091090 (E-Woo Technology, 2010) after a 134-day review. Its family tree reaches back 8 generations to 1998. 13 later devices descend from it.

Decided
Jan 15, 2015
Review
134 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K981556 (1998). 14 ancestors in all. 13 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor2006: 2 other ancestors2003: 1 other ancestor2001: 1 other ancestor2000: 1 other ancestor2016: 2 descendants cleared2015: 1 descendant cleared2019: 3 descendants cleared2017: 1 descendant cleared2022: 1 descendant cleared2023: 2 descendants cleared2025: 2 descendants cleared2024: 1 descendant clearedK981556 · Canon X-Ray Digital Camera Cxdi-11 · Canon USA, Inc. · 1998K992547 · Canon X-Ray Digital Camera, Model Cxdi-22 · Canon USA, Inc. · 1999K023750 · Cannon Digital Radiography Model Cxdi-40G · Canon USA, Inc. · 2002K031447 · Canon, Digital Radiography, Model Cxdi-50G · Canon, Inc. · 2003K042876 · Urs LP Digital, Millennium, Radpro · Sedecal., Sa. · 2004K090238 · Sedecal X-Plus LP Plus Digital Diagnostic X-Ray Systems · Sedecal., Sa. · 2009×2: 2 generations cleared close together, K092830 (2010), K091090 (2010) 1995200020052010201520202025
  1. Root · 8 generations backK981556 Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc. · 1998
  2. 7 generations backK992547 Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc. · 1999
  3. 6 generations backK023750 Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc. · 2002
  4. 5 generations backK031447 Canon, Digital Radiography, Model Cxdi-50GCanon, Inc. · 2003
  5. 4 generations backK042876 Urs LP Digital, Millennium, RadproSedecal., Sa. · 2004
  6. 3 generations backK090238 Sedecal X-Plus LP Plus Digital Diagnostic X-Ray SystemsSedecal., Sa. · 2009
  7. 2 generations backK092830 Digital X-Ray Imaging System, Model DRC-1000VATECH Co., Ltd. · 2010
  8. 1 generation backK091090 Digital Flat Panel X-Ray Detector, Model Xmaru 1717E-Woo Technology · 2010
  9. This deviceK142475 EVS 4343DRTECH Corporation · 2015
  10. Descendant · cites it directly · 7 of its ownK162555 Evs 4343, Evs 4343GDRTECH Corporation · 2016
  11. Descendant · 2 generations on · 6 of its ownK192400 Evs 4343A, Evs 4343AG, Evs 3643A, Evs 3643AGDRTECH Corporation · 2019
  12. Descendant · cites it directly · 4 of its ownK151942 EVS 3643DRTECH Corporation · 2015
  13. Descendant · 2 generations on · 3 of its ownK162552 Evs 3643, Evs 3643GDRTECH Corporation · 2016
  14. Descendant · 3 generations on · 2 of its ownK223124 Expd 86P, Expd 86PG, Expd 129P, Expd 129PGDRTECH Corporation · 2022

Showing 5 of 13 descendants. See all descendants

Descendants cleared per year

2015: 12016: 22017: 12019: 32022: 12023: 22024: 12025: 2
2015high 3 (2019) · low 0 (2018)2026

Most influential descendants

Showing 5 of 13 · See all
  • K162555Evs 4343, Evs 4343GDRTECH Corporation · 2016 · cites it directly7descendants
  • K192400Evs 4343A, Evs 4343AG, Evs 3643A, Evs 3643AGDRTECH Corporation · 2019 · 2 generations on6descendants
  • K151942EVS 3643DRTECH Corporation · 2015 · cites it directly4descendants
  • K162552Evs 3643, Evs 3643GDRTECH Corporation · 2016 · 2 generations on3descendants
  • K223124Expd 86P, Expd 86PG, Expd 129P, Expd 129PGDRTECH Corporation · 2022 · 3 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K981556Canon X-Ray Digital Camera Cxdi-11Canon USA, Inc.1998—
−7K992547Canon X-Ray Digital Camera, Model Cxdi-22Canon USA, Inc.1999—
−6K023750Cannon Digital Radiography Model Cxdi-40GCanon USA, Inc.2002—
−5K031447Canon, Digital Radiography, Model Cxdi-50GCanon, Inc.2003—
−4K042876Urs LP Digital, Millennium, RadproSedecal., Sa.2004—
−3K090238Sedecal X-Plus LP Plus Digital Diagnostic X-Ray SystemsSedecal., Sa.2009—
−2K092830Digital X-Ray Imaging System, Model DRC-1000VATECH Co., Ltd.2010—
−1K091090Digital Flat Panel X-Ray Detector, Model Xmaru 1717E-Woo Technology2010—
0 (this device)K142475EVS 4343DRTECH Corporation2015—
+1K162555Evs 4343, Evs 4343GDRTECH Corporation2016—
+2K192400Evs 4343A, Evs 4343AG, Evs 3643A, Evs 3643AGDRTECH Corporation2019—
+1K151942EVS 3643DRTECH Corporation2015—
+2K162552Evs 3643, Evs 3643GDRTECH Corporation2016—
+3K223124Expd 86P, Expd 86PG, Expd 129P, Expd 129PGDRTECH Corporation2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010
200110
200210
200310
200620

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201620
201710
201930
202210
202320
202410
202520
FIG. 1 — Lineage of K142475, 1998–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K201528 Yushan X-Ray Flat Panel Detector with DROCscore 21.5 · 12 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K091090Digital Flat Panel X-Ray Detector, Model Xmaru 1717
Summary page 4
…: MQB • Device Class: II 4. Identification of Predicate Device(s) [21 CFR 807.92(a) (3)] • 510(k) Number: K091090 • Applicant: E-WOO TECHNOLIGY • Trade Name: Xmaru1717 • Common Name:…
E-Woo Technology2010—

Also cleared against K091090: 2 other devices →

What descends from it? (13)

See all 13

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

NumberDeviceApplicantDecidedDescendants
K162555Evs 4343, Evs 4343GDRTECH Corporation20167
K151942EVS 3643DRTECH Corporation20154

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 17 years and passes through 6 companies; a new generation was cleared every 1.5 years on median.
  • 1 of the 14 ancestors has a recall of any class.
  • Of its descendants, K162555 (DRTECH Corporation, 2016) has gone furthest, with 7 descendants of its own.
  • 2 other devices also cite its predicate K091090.

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. 2015, this device’s year, is highlighted.

FDA decisions per year · MQB

8in 2025

2007: 132008: 82009: 152010: 112011: 242012: 222013: 212014: 322015: 212016: 222017: 312018: 162019: 222020: 192021: 212022: 312023: 102024: 82025: 82026 (partial year): 3
2007high 32 (2014) · low 8 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQB

127in 2025

2007: 22 days median2008: 15 days median2009: 57 days median2010: 116 days median2011: 102 days median2012: 80 days median2013: 105 days median2014: 102 days median2015: 81 days median2016: 92 days median2017: 30 days median2018: 30 days median2019: 30 days median2020: 28 days median2021: 48 days median2022: 48 days median2023: 30 days median2024: 187 days median2025: 127 days median2026 (partial year): 245 days median
2007high 245 (2026) · low 15 (2008)2026

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

Recalls per year · MQB

1in 2025

2007: 152008: 362009: 192010: 142011: 102012: 82013: 62017: 12018: 42019: 12020: 42021: 12025: 12026 (partial year): 1
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

2007: 252008: 302009: 342010: 392011: 1012012: 2672013: 1592014: 292015: 212016: 262017: 202018: 842019: 452020: 92021: 262022: 132023: 512024: 912025: 141
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
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200713221525
20088153630
200915571934
2010111161439
20112410210101
201222808267
2013211056159
201432102029
20152181021
20162292026
20173130120
20181630484
20192230145
2020192849
20212148126
20223148013
20231030051
20248187091
202581271141
202632451—

What is it indicated for?

The EVS 4343 Digital X-ray detector is indicated for digital imaging solution designed for providing general radiographic diagnosis of human anatomy. This device is intended to replace film or screen based radiographic systems in all general purpose diagnostic procedures. This device is not intended for mammography applications

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K142475: EVS 4343.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142475

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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