510(k) · Cleared
ClearedX-ray Flat Panel Detectors (EverestView 4343X)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Careray Digital Medical Technology Co., Ltd. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Cleared on Dec 30, 2022 as substantially equivalent to K221549 (Careray Digital Medical Technology Co., Ltd., 2022) after a 21-day review. Its family tree reaches back 12 generations to 1981. 1 later device descends from it.
- Decided
- Dec 30, 2022
- Review
- 21 days
- Class
- Class II
- Product code
- MQB
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 12 generations to K803130 (1981). 29 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 12 generations backK803130 Multix U. Bucky Table X-Ray UnitSiemens Corp. · 1981 · Recalled
- 8 generations between
- 3 generations backK153492 CareView 1800LCareray Digital Medical System Co., Ltd. · 2015
- 2 generations backK193173 CareView 1800LeCareray Digital Medical System Co., Ltd. · 2019
- 1 generation backK221549 X-ray Flat Panel Detectors (CareView 1800 RF)Careray Digital Medical Technology Co., Ltd. · 2022
- This deviceK223687 X-ray Flat Panel Detectors (EverestView 4343X)Careray Digital Medical Technology Co., Ltd. · 2022
- Descendant · cites it directly · 0 of its ownK232058 YosemiteView 4343W/YosemiteView 3643WCareray Digital Medical Technology Co., Ltd. · 2023
Show all 12 generations
- Root · 12 generations backK803130 Multix U. Bucky Table X-Ray UnitSiemens Corp. · 1981 · Recalled
- 11 generations backK971452 Multix Top/Pro Radiographic X-Ray TableSiemens Medical Solutions USA, Inc. · 1997 · Recalled
- 10 generations backK983732 Thorax FD and Multix FDSiemens Medical Solutions USA, Inc. · 1999 · Recalled
- 9 generations backK992794 Stingray DR, Model 1Infimed, Inc. · 1999
- 8 generations backK024147 Paxscan 4030 Medical Digital Imaging SystemVarian Medical Systems, Inc. · 2003
- 7 generations backK120020 Vivix-SVieworks Co., Ltd. · 2012
- 6 generations backK122865 Vivix-S WirelessVieworks Co., Ltd. · 2013
- 5 generations backK150929 CareView 1500Cw X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd. · 2015
- 4 generations backK153058 CareView 1500C/ CareView 1500L X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd. · 2015
- 3 generations backK153492 CareView 1800LCareray Digital Medical System Co., Ltd. · 2015
- 2 generations backK193173 CareView 1800LeCareray Digital Medical System Co., Ltd. · 2019
- 1 generation backK221549 X-ray Flat Panel Detectors (CareView 1800 RF)Careray Digital Medical Technology Co., Ltd. · 2022
- This deviceK223687 X-ray Flat Panel Detectors (EverestView 4343X)Careray Digital Medical Technology Co., Ltd. · 2022
Most influential descendants
Showing 1 of 1 · See all- K232058YosemiteView 4343W/YosemiteView 3643WCareray Digital Medical Technology Co., Ltd. · 2023 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −12 | K803130 | Multix U. Bucky Table X-Ray Unit | Siemens Corp. | 1981 | 1 |
| −11 | K971452 | Multix Top/Pro Radiographic X-Ray Table | Siemens Medical Solutions USA, Inc. | 1997 | 8 |
| −10 | K983732 | Thorax FD and Multix FD | Siemens Medical Solutions USA, Inc. | 1999 | 1 |
| −9 | K992794 | Stingray DR, Model 1 | Infimed, Inc. | 1999 | — |
| −8 | K024147 | Paxscan 4030 Medical Digital Imaging System | Varian Medical Systems, Inc. | 2003 | — |
| −7 | K120020 | Vivix-S | Vieworks Co., Ltd. | 2012 | — |
| −6 | K122865 | Vivix-S Wireless | Vieworks Co., Ltd. | 2013 | — |
| −5 | K150929 | CareView 1500Cw X-ray Flat Panel Detectors | Careray Digital Medical System Co., Ltd. | 2015 | — |
| −4 | K153058 | CareView 1500C/ CareView 1500L X-ray Flat Panel Detectors | Careray Digital Medical System Co., Ltd. | 2015 | — |
| −3 | K153492 | CareView 1800L | Careray Digital Medical System Co., Ltd. | 2015 | — |
| −2 | K193173 | CareView 1800Le | Careray Digital Medical System Co., Ltd. | 2019 | — |
| −1 | K221549 | X-ray Flat Panel Detectors (CareView 1800 RF) | Careray Digital Medical Technology Co., Ltd. | 2022 | — |
| 0 (this device) | K223687 | X-ray Flat Panel Detectors (EverestView 4343X) | Careray Digital Medical Technology Co., Ltd. | 2022 | — |
| +1 | K232058 | YosemiteView 4343W/YosemiteView 3643W | Careray Digital Medical Technology Co., Ltd. | 2023 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1986 | 1 | 0 |
| 1988 | 1 | 0 |
| 1992 | 1 | 0 |
| 1994 | 2 | 0 |
| 1995 | 2 | 0 |
| 1997 | 1 | 0 |
| 1998 | 3 | 0 |
| 1999 | 1 | 0 |
| 2000 | 1 | 0 |
| 2002 | 2 | 0 |
| 2003 | 1 | 0 |
| 2009 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2023 | 1 | 0 |
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
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K221549 | X-ray Flat Panel Detectors (CareView 1800 RF)Summary page 5…ulation Number: 21 CFR 892.1680 Regulatory Class: Class II Product Code: MQB,JAA FDA 510(k) #: K221549 5. Description of the Device [21 CFR 807.92(a)(4)] The detector functions by intercepting X-ray photons. Then the scintillato… | 2022 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K232058 | YosemiteView 4343W/YosemiteView 3643W | 2023 | 0 |
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 41 years and passes through 7 companies; a new generation was cleared every 2.5 years on median.
- 10 of the 29 ancestors have a recall of any class.
- Of its descendants, K232058 (Careray Digital Medical Technology Co., Ltd., 2023) has gone furthest, with 0 descendants of its own.
How does its category compare?
All MQB devicesMQB 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
2026 to Oct 25, outlined.
Median 510(k) review, days · MQB
127in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MQB
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MQB
141in 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?
The detector is indicated for digital imaging solution designed for providing general radiographic diagnosis of human anatomy. It is intended to replace radiographic film/screen systems in all general-purpose diagnostic procedures. This product is not intended for mammography applications.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K223687 · printed Nov 5, 2026
Cite this page
510(k) Report. “K223687: X-ray Flat Panel Detectors (EverestView 4343X).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K223687
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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