510(k) Report

510(k) · Cleared

Cleared

21.3 inch (54 cm) Color Digital Mammography LCD Monitor CCL550i2(CL21550)

K151007510(k) TraditionalCleared May 8, 201523-day reviewClass II21 CFR 892.2050

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

Jvckenwood Corporation · PGY Display, Diagnostic Radiology

Cleared on May 8, 2015 as substantially equivalent to K131137 (Jvckenwood Corporation, 2013) after a 23-day review. Its family tree reaches back 9 generations to 1991.

Decided
May 8, 2015
Review
23 days
Class
Class II
Product code
PGY
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K913770 (1991). 21 ancestors in all, the oldest K885042 (1988). No later device cites it as a predicate yet.

  1. Root · 9 generations backK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
  2. 5 generations between
  3. 3 generations backK061447 5M Monochrome Digital Mammography LCD Monitor MDL2116A (ME551I2)Totoku Electric Co., Ltd. · 2006
  4. 2 generations backK111496 21.3 Inch (54CM) Monochrome Digital Mammography LCD MonitorTotoku Electric Co., Ltd. · 2011
  5. 1 generation backK131137 21.3 Inch Monochrome Digital Mammography LCD Monitor MS55I2…Jvckenwood Corporation · 2013
  6. This deviceK151007 21.3 inch (54 cm) Color Digital Mammography LCD Monitor…Jvckenwood Corporation · 2015
Show all 9 generations
  1. Root · 9 generations backK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
  2. 8 generations backK960613 GE Advantage Windows Review WorkstationGE Medical Systems · 1996
  3. 7 generations backK972701 Barco MWD 321 Medical Workstation DisplayBarco NV Display Systems · 1998
  4. 6 generations backK980541 Barco MGD 521 5 Megapixel Diagnostic DisplayBarco NV Display Systems · 1998
  5. 5 generations backK033859 Barcoview MGD 521M Digital Mammography DisplayBarco NV Barcoview · 2004
  6. 4 generations backK041737 5M Monochrome Digital Mammography LCD Monitor ME511L (MDL2105A)Totoku Electric Co., Ltd. · 2004
  7. 3 generations backK061447 5M Monochrome Digital Mammography LCD Monitor MDL2116A (ME551I2)Totoku Electric Co., Ltd. · 2006
  8. 2 generations backK111496 21.3 Inch (54CM) Monochrome Digital Mammography LCD MonitorTotoku Electric Co., Ltd. · 2011
  9. 1 generation backK131137 21.3 Inch Monochrome Digital Mammography LCD Monitor MS55I2…Jvckenwood Corporation · 2013
  10. This deviceK151007 21.3 inch (54 cm) Color Digital Mammography LCD Monitor…Jvckenwood Corporation · 2015
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K913770Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co.1991—
−8K960613GE Advantage Windows Review WorkstationGE Medical Systems1996—
−7K972701Barco MWD 321 Medical Workstation DisplayBarco NV Display Systems1998—
−6K980541Barco MGD 521 5 Megapixel Diagnostic DisplayBarco NV Display Systems1998—
−5K033859Barcoview MGD 521M Digital Mammography DisplayBarco NV Barcoview2004—
−4K0417375M Monochrome Digital Mammography LCD Monitor ME511L (MDL2105A)Totoku Electric Co., Ltd.2004—
−3K0614475M Monochrome Digital Mammography LCD Monitor MDL2116A (ME551I2)Totoku Electric Co., Ltd.2006—
−2K11149621.3 Inch (54CM) Monochrome Digital Mammography LCD MonitorTotoku Electric Co., Ltd.2011—
−1K13113721.3 Inch Monochrome Digital Mammography LCD Monitor MS55I2 (ML21055, MD211G5)Jvckenwood Corporation2013—
0 (this device)K15100721.3 inch (54 cm) Color Digital Mammography LCD Monitor CCL550i2(CL21550)Jvckenwood Corporation2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199020
199110
199410
199520
199640
199710
FIG. 1 — Lineage of K151007, 1991–2015Source: 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 PGY? 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 PGY device

  1. #1 K261213 Medical Monitor (40HT513D)score 13.9 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K13113721.3 Inch Monochrome Digital Mammography LCD Monitor MS55I2 (ML21055, MD211G5)
Summary page 4
…ication System) Predicate Device: 21.3 inch (54 cm) inch Monochrome Digital Mammography LCD Monitor MS55i2 (ML21055) (K131137) Device Description: CCL550i2 (CL21550) is a 21.3 inch (54 cm) color LCD monito…
Jvckenwood Corporation2013—

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 24 years and passes through 6 companies; a new generation was cleared every 1.8 years on median.
  • None of the 21 ancestors has a recall.

How does its category compare?

All PGY devices

PGY Display, Diagnostic Radiology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · PGY

3in 2025

2014: 142015: 162016: 182017: 112018: 52019: 112020: 122021: 72022: 102023: 172024: 102025: 32026 (partial year): 4
2007high 18 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PGY

59in 2025

2014: 24 days median2015: 31 days median2016: 27 days median2017: 30 days median2018: 28 days median2019: 58 days median2020: 61 days median2021: 77 days median2022: 60 days median2023: 60 days median2024: 53 days median2025: 59 days median2026 (partial year): 48 days median
2007high 77 (2021) · low 24 (2014)2026

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

Recalls per year · PGY

No recall names PGY since 2007.

Adverse event reports per year · PGY

1in 2017

2017: 1
2007high 1 (2017) · low 0 (2007)2025

MAUDE reports naming product code PGY, 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
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
2014142400
2015163100
2016182700
2017113001
201852800
2019115800
2020126100
202177700
2022106000
2023176000
2024105300
202535900
20264480—

What is it indicated for?

21.3 inch (54 cm) inch Color Digital Mammography 5M pixel LCD Monitor CCL550i2 (CL21550) is intended to be used in displaying and viewing medical images for diagnosis by trained medical practitioners. It is to be used in digital mammography PACS and modalities including FFDM.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151007: 21.3 inch (54 cm) Color Digital Mammography LCD Monitor CCL550i2(CL21550).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K151007

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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