510(k) Report

510(k) · Cleared

Cleared

Universal DR 1748

K214030510(k) TraditionalCleared Jan 21, 202229-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

Konica Minolta Healthcare Americas, Inc. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Jan 21, 2022 as substantially equivalent to K210919 (Radmedix, LLC, 2021) after a 29-day review. Its family tree reaches back 14 generations to 1990. 1 later device descends from it.

Decided
Jan 21, 2022
Review
29 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 14 generations to K896095 (1990). 26 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 14 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
  2. 10 generations between
  3. 3 generations backK200726 AcuityPDRRadmedix, LLC · 2020
  4. 2 generations backK201058 Accuvue+Radmedix, LLC · 2020
  5. 1 generation backK210919 AcuityDReRadmedix, LLC · 2021
  6. This deviceK214030 Universal DR 1748Konica Minolta Healthcare Americas, Inc. · 2022
  7. Descendant · cites it directly · 0 of its ownK252996 Universal 1417PIKonica Minolta Healthcare Americas, Inc. · 2026
Show all 14 generations
  1. Root · 14 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
  2. 13 generations backK962699 Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V. · 1996
  3. 12 generations backK982862 Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V. · 1998
  4. 11 generations backK012211 Efilm WorkstationEfilm Medical, Inc. · 2001 · Recalled
  5. 10 generations backK020995 Efilm Workstation with ModulesEfilm Medical, Inc. · 2002 · Recalled
  6. 9 generations backK070618 Dicompacs, Model 5Oehm Und Rehbein GmbH · 2007
  7. 8 generations backK091364 Dicompacs, Model 5.2, Dicompacs DX-R, Model 1.4Oehm Und Rehbein GmbH · 2009
  8. 7 generations backK100449 Minxray Model CMDR-2SMinxray, Inc. · 2010
  9. 6 generations backK141885 CMDR-2ST & CMDR-2SLWT Digital Portable X-RayMinxray, Inc. · 2014
  10. 5 generations backK171353 CMDR 2ST (Multiple Models), CMDR 2SPE (Multiple Models), IntegrisMinxray, Inc. · 2017
  11. 4 generations backK191451 CMDR 2CW (Multiple models)Minxray, Inc. · 2019
  12. 3 generations backK200726 AcuityPDRRadmedix, LLC · 2020
  13. 2 generations backK201058 Accuvue+Radmedix, LLC · 2020
  14. 1 generation backK210919 AcuityDReRadmedix, LLC · 2021
  15. This deviceK214030 Universal DR 1748Konica Minolta Healthcare Americas, Inc. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−14K896095Images-on-Call Teleradiology SystemDevices & Services Co.1990—
−13K962699Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V.1996—
−12K982862Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V.1998—
−11K012211Efilm WorkstationEfilm Medical, Inc.20011
−10K020995Efilm Workstation with ModulesEfilm Medical, Inc.20022
−9K070618Dicompacs, Model 5Oehm Und Rehbein GmbH2007—
−8K091364Dicompacs, Model 5.2, Dicompacs DX-R, Model 1.4Oehm Und Rehbein GmbH2009—
−7K100449Minxray Model CMDR-2SMinxray, Inc.2010—
−6K141885CMDR-2ST & CMDR-2SLWT Digital Portable X-RayMinxray, Inc.2014—
−5K171353CMDR 2ST (Multiple Models), CMDR 2SPE (Multiple Models), IntegrisMinxray, Inc.2017—
−4K191451CMDR 2CW (Multiple models)Minxray, Inc.2019—
−3K200726AcuityPDRRadmedix, LLC2020—
−2K201058Accuvue+Radmedix, LLC2020—
−1K210919AcuityDReRadmedix, LLC2021—
0 (this device)K214030Universal DR 1748Konica Minolta Healthcare Americas, Inc.2022—
+1K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199810
199910
200110
200230
200310
200410
200510
200810
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K214030, 1990–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
*K210919AcuityDRe
Summary page 4
…ially equivalent device: Trade Name: SKR 3000 Manufacturer: Konica Minolta Healthcare Americas, Inc 510(k) #: K210919 Classification Name: Stationary x-ray system Classification Panel: Radiology Classification Regulatio…
Radmedix, LLC2021—
†K212291PhoenixSedecal., Sa.20211

Also cleared against K210919: 1 other device →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.20260

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 32 years and passes through 7 companies; a new generation was cleared every 2.2 years on median.
  • 3 of the 26 ancestors have a recall of any class.
  • Of its descendants, K252996 (Konica Minolta Healthcare Americas, Inc., 2026) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K210919.

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. 2022, 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?

This device is indicated for use in generating radiographic images of human anatomy. It is intended to a replace radiographic film/screen system in general-purpose diagnostic procedures. This device is not indicated for use in mammography, fluoroscopy, and angiography applications.

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

Cite this page

510(k) Report. “K214030: Universal DR 1748.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K214030

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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