510(k) Report

510(k) · Cleared

Cleared

X-ray Flat Panel Detectors (CareView 1800Cwe /CareView 1500Cwe)

K201932510(k) SpecialCleared Aug 7, 202025-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

Careray Digital Medical System Co., Ltd. · MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Cleared on Aug 7, 2020 as substantially equivalent to K193173 (Careray Digital Medical System Co., Ltd., 2019) after a 25-day review. Its family tree reaches back 11 generations to 1981.

Decided
Aug 7, 2020
Review
25 days
Class
Class II
Product code
MQB
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K803130 (1981). 28 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 11 generations backK803130 Multix U. Bucky Table X-Ray UnitSiemens Corp. · 1981 · Recalled
  2. 7 generations between
  3. 3 generations backK153058 CareView 1500C/ CareView 1500L X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd. · 2015
  4. 2 generations backK153492 CareView 1800LCareray Digital Medical System Co., Ltd. · 2015
  5. 1 generation backK193173 CareView 1800LeCareray Digital Medical System Co., Ltd. · 2019
  6. This deviceK201932 X-ray Flat Panel Detectors (CareView 1800Cwe /CareView 1500Cwe)Careray Digital Medical System Co., Ltd. · 2020
Show all 11 generations
  1. Root · 11 generations backK803130 Multix U. Bucky Table X-Ray UnitSiemens Corp. · 1981 · Recalled
  2. 10 generations backK971452 Multix Top/Pro Radiographic X-Ray TableSiemens Medical Solutions USA, Inc. · 1997 · Recalled
  3. 9 generations backK983732 Thorax FD and Multix FDSiemens Medical Solutions USA, Inc. · 1999 · Recalled
  4. 8 generations backK992794 Stingray DR, Model 1Infimed, Inc. · 1999
  5. 7 generations backK024147 Paxscan 4030 Medical Digital Imaging SystemVarian Medical Systems, Inc. · 2003
  6. 6 generations backK120020 Vivix-SVieworks Co., Ltd. · 2012
  7. 5 generations backK122865 Vivix-S WirelessVieworks Co., Ltd. · 2013
  8. 4 generations backK150929 CareView 1500Cw X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd. · 2015
  9. 3 generations backK153058 CareView 1500C/ CareView 1500L X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd. · 2015
  10. 2 generations backK153492 CareView 1800LCareray Digital Medical System Co., Ltd. · 2015
  11. 1 generation backK193173 CareView 1800LeCareray Digital Medical System Co., Ltd. · 2019
  12. This deviceK201932 X-ray Flat Panel Detectors (CareView 1800Cwe /CareView 1500Cwe)Careray Digital Medical System Co., Ltd. · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K803130Multix U. Bucky Table X-Ray UnitSiemens Corp.19811
−10K971452Multix Top/Pro Radiographic X-Ray TableSiemens Medical Solutions USA, Inc.19978
−9K983732Thorax FD and Multix FDSiemens Medical Solutions USA, Inc.19991
−8K992794Stingray DR, Model 1Infimed, Inc.1999—
−7K024147Paxscan 4030 Medical Digital Imaging SystemVarian Medical Systems, Inc.2003—
−6K120020Vivix-SVieworks Co., Ltd.2012—
−5K122865Vivix-S WirelessVieworks Co., Ltd.2013—
−4K150929CareView 1500Cw X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd.2015—
−3K153058CareView 1500C/ CareView 1500L X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd.2015—
−2K153492CareView 1800LCareray Digital Medical System Co., Ltd.2015—
−1K193173CareView 1800LeCareray Digital Medical System Co., Ltd.2019—
0 (this device)K201932X-ray Flat Panel Detectors (CareView 1800Cwe /CareView 1500Cwe)Careray Digital Medical System Co., Ltd.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198810
199210
199420
199520
199710
199830
199910
200010
200220
200310
200910
FIG. 1 — Lineage of K201932, 1981–2020Source: 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
*K193173CareView 1800Le
Summary page 6
…Page 2 of 7 Regulatory Class: Class II Product Code: MQB FDA 510(k) #: K193173 5. Description of the Device [21 CFR 807.92(a)(4)] The CareView 1800Cwe/ CareView 1500Cwe detector is a class of digital…
Careray Digital Medical System Co., Ltd.2019—

Also cleared against K193173: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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 39 years and passes through 6 companies; a new generation was cleared every 1.9 years on median.
  • 10 of the 28 ancestors have a recall of any class.
  • 1 other device also cites its predicate K193173.

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. 2020, 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 CareView 1800Cwe/ CareView 1500Cwe 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.

Cite this page

510(k) Report. “K201932: X-ray Flat Panel Detectors (CareView 1800Cwe /CareView 1500Cwe).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201932

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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