510(k) Report

510(k) · Cleared

Cleared

Sectra IDS5 Workstation

K050196510(k) SpecialCleared Feb 24, 200528-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

Sectra Imtec AB · LLZ System, Image Processing, Radiological

Cleared on Feb 24, 2005 as substantially equivalent to K040376 (Sectra-Imtec AB, 2004) after a 28-day review. Its family tree reaches back 2 generations to 2003. 36 later devices descend from it.

Decided
Feb 24, 2005
Review
28 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K033712 (2003). 36 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2012: 1 descendant cleared2005: 1 descendant cleared2008: 3 descendants cleared2006: 1 descendant cleared2013: 4 descendants cleared2010: 1 descendant cleared2014: 2 descendants cleared2007: 1 descendant cleared2016: 3 descendants cleared2015: 2 descendants cleared2018: 5 descendants cleared2017: 1 descendant cleared2020: 2 descendants cleared2021: 4 descendants cleared2023: 1 descendant cleared2022: 1 descendant cleared2024: 2 descendants cleared2025: 1 descendant clearedK033712 · Modification to Sectra IDS5 Radiology Workstation - Version 10.1 · Sectra-Imtec AB · 2003K040376 · Sectra IDS5 Radiology Workstation; Sectra MPR Package; Sectra 3D Package · Sectra-Imtec AB · 2004200020052010201520202025
Descendants, by generation 1 generation forward: 3 descendants2 generations forward: 5 descendants3 generations forward: 9 descendants4 generations forward: 10 descendants5 generations forward: 5 descendants6 generations forward: 3 descendants7 generations forward: 1 descendant K040376 · Sectra IDS5 Radiology Workstation; Sectra MPR Package; Sectra 3D Package · Sectra-Imtec AB · 2004K033712 · Modification to Sectra IDS5 Radiology Workstation - Version 10.1 · Sectra-Imtec AB · 20030+5
  1. Root · 2 generations backK033712 Modification to Sectra IDS5 Radiology Workstation - Version 10.1Sectra-Imtec AB · 2003
  2. 1 generation backK040376 Sectra IDS5 Radiology Workstation; Sectra MPR Package; Sectra 3D…Sectra-Imtec AB · 2004
  3. This deviceK050196 Sectra IDS5 WorkstationSectra Imtec AB · 2005
  4. Descendant · cites it directly · 35 of its ownK051315 Modification to: Sectra IDS5 WorkstationSectra Imtec AB · 2005 · Recalled
  5. Descendant · 2 generations on · 34 of its ownK063093 Sectra Workstation, Version 11.1Sectra Imtec AB · 2006 · Recalled
  6. Descendant · 3 generations on · 27 of its ownK073272 Workstationone Breast Imaging WorkstationThree Palm Software, LLC · 2007
  7. Descendant · cites it directly · 25 of its ownK082483 QuantraHologic, Inc. · 2008
  8. Descendant · 2 generations on · 24 of its ownK102556 Volpara, Version 1.3Matakina Technology Limited · 2010

Showing 5 of 36 descendants. See all descendants

Descendants cleared per year

2005: 12006: 12007: 12008: 32010: 12012: 12013: 42014: 22015: 22016: 32017: 12018: 52020: 22021: 42022: 12023: 12024: 22025: 1
2005high 5 (2018) · low 0 (2009)2026

Most influential descendants

Showing 5 of 36 · See all
  • K051315Modification to: Sectra IDS5 WorkstationSectra Imtec AB · 2005 · cites it directly35descendants
  • K063093Sectra Workstation, Version 11.1Sectra Imtec AB · 2006 · 2 generations on34descendants
  • K073272Workstationone Breast Imaging WorkstationThree Palm Software, LLC · 2007 · 3 generations on27descendants
  • K082483QuantraHologic, Inc. · 2008 · cites it directly25descendants
  • K102556Volpara, Version 1.3Matakina Technology Limited · 2010 · 2 generations on24descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K033712Modification to Sectra IDS5 Radiology Workstation - Version 10.1Sectra-Imtec AB2003—
−1K040376Sectra IDS5 Radiology Workstation; Sectra MPR Package; Sectra 3D PackageSectra-Imtec AB2004—
0 (this device)K050196Sectra IDS5 WorkstationSectra Imtec AB2005—
+1K051315Modification to: Sectra IDS5 WorkstationSectra Imtec AB20051
+2K063093Sectra Workstation, Version 11.1Sectra Imtec AB20061
+3K073272Workstationone Breast Imaging WorkstationThree Palm Software, LLC2007—
+1K082483QuantraHologic, Inc.2008—
+2K102556Volpara, Version 1.3Matakina Technology Limited2010—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
200610
200710
200830
201010
201210
201340
201420
201520
201630
201710
201850
202020
202140
202210
202310
202420
202510
FIG. 1 — Lineage of K050196, 2003–2025Source: 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 LLZ? 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 LLZ device

  1. #1 K230955 syngo Application Softwarescore 21.5 · 11 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
*K040376Sectra IDS5 Radiology Workstation; Sectra MPR Package; Sectra 3D Package
Summary page 1
…Classification Name: Image Processing System (LLZ) (21 CFR § 892.2050) Predicate Device: Applicant: Sectra Imtec AB 5 10(k) Number: K040376 Device: Sectra IDS5 Workstation Device Description: The Sectra HDS5 Workstation is mainly a software…
Sectra-Imtec AB2004—

Also cleared against K040376: 6 other devices →

What descends from it? (36)

See all 36

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

NumberDeviceApplicantDecidedDescendants
K051315Modification to: Sectra IDS5 WorkstationSectra Imtec AB200535
K082483QuantraHologic, Inc.200825
K120472QuantraHologic, Inc.20123

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 2 years and passes through 2 companies; a new generation was cleared every 10 months on median.
  • None of the 2 ancestors has a recall.
  • Of its descendants, K051315 (Sectra Imtec AB, 2005) has gone furthest, with 35 descendants of its own.
  • 6 other devices also cite its predicate K040376.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LLZ

58in 2025

2007: 762008: 942009: 702010: 512011: 1062012: 822013: 952014: 782015: 642016: 822017: 782018: 1042019: 742020: 812021: 832022: 652023: 872024: 622025: 582026 (partial year): 45
2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007: 36 days median2008: 52 days median2009: 62 days median2010: 98 days median2011: 79 days median2012: 87 days median2013: 84 days median2014: 89 days median2015: 90 days median2016: 90 days median2017: 107 days median2018: 105 days median2019: 107 days median2020: 115 days median2021: 116 days median2022: 137 days median2023: 157 days median2024: 131 days median2025: 173 days median2026 (partial year): 110 days median
2007high 173 (2025) · low 36 (2007)2026

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

Recalls per year · LLZ

11in 2025

2007: 202008: 322009: 212010: 172011: 302012: 122013: 642014: 62015: 162016: 122017: 52018: 72019: 22020: 62021: 32022: 42023: 82024: 62025: 112026 (partial year): 14
2007high 64 (2013) · low 2 (2019)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LLZ

116in 2025

2007: 1522008: 1542009: 1452010: 1452011: 4542012: 2662013: 1,1302014: 15,6312015: 2112016: 2902017: 1042018: 722019: 882020: 822021: 702022: 282023: 262024: 422025: 116
2007high 15,631 (2014) · low 26 (2023)2025

MAUDE reports naming product code LLZ, 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
2007763620152
2008945232154
2009706221145
2010519817145
20111067930454
2012828712266
20139584641,130
20147889615,631
2015649016211
2016829012290
2017781075104
2018104105772
201974107288
202081115682
202183116370
202265137428
202387157826
202462131642
20255817311116
20264511014—

What is it indicated for?

The Sectra IDS5 device is intended for the manipulation and displaying of medical images, including mammograms. It can show images from different modalities and interfaces to various image storage and printing devices using DICOM or similar interface standards. Device options make possible mammography reading, telecommunications; fast demonstration; prosthesis CAD; 3-D and angiography, etc.; and teleconferencing. Lossy compressed mammographic images are…

Read the full statement (101 words)

The Sectra IDS5 device is intended for the manipulation and displaying of medical images, including mammograms. It can show images from different modalities and interfaces to various image storage and printing devices using DICOM or similar interface standards.

Device options make possible mammography reading, telecommunications; fast demonstration; prosthesis CAD; 3-D and angiography, etc.; and teleconferencing.

Lossy compressed mammographic images are not intended for diagnostic review. Mammographic images should only be viewed with a monitor approved by FDA for viewing mammographic images.

Typical users of this system are trained professionals, including but not limited to physicians, radiologists, nurses, medical technicians, and assistants.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K050196: Sectra IDS5 Workstation.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K050196

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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