510(k) · Cleared
ClearedCollaboration Live
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Philips Health Care · LLZ System, Image Processing, Radiological
Cleared on Feb 18, 2020 as substantially equivalent to K150193 (Ge Medical Systems, LLC, 2015) after a 25-day review. Its family tree reaches back 6 generations to 1997. 4 later devices descend from it.
- Decided
- Feb 18, 2020
- Review
- 25 days
- Class
- Class II
- Product code
- LLZ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K971684 (1997). 29 ancestors in all, the oldest K871859 (1987). 4 later devices descend from it, 2 citing it directly.
- Root · 6 generations backK971684 Magnetom Project 047 System (Numaris 3.5 Software)Siemens Medical Solutions USA, Inc. · 1997 · Recalled
- 5 generations backK032428 Magnetom Avanto MR SystemSiemens Medical Solutions USA, Inc. · 2003 · Recalled
- 4 generations backK041112 Magnetom Espree SystemSiemens Medical Solutions USA, Inc. · 2004 · Recalled
- 3 generations backK052423 Magnetom Systems with Syngo Expert - I OptionSiemens Medi Cal Solutions, Inc. · 2006
- 2 generations backK061449 Syngo Expert-1Siemens Medical Solution · 2006
- 1 generation backK150193 Customer Remote Console (CRC)Ge Medical Systems, LLC · 2015
- This deviceK200179 Collaboration LivePhilips Health Care · 2020
- Descendant · cites it directly · 2 of its ownK201665 Collaboration LivePhilips Ultrasound, Inc. · 2020
- Descendant · 2 generations on · 1 of its ownK212777 Collaboration LivePhilips Ultrasound, Inc. · 2021
- Descendant · cites it directly · 0 of its ownK242329 CT Collaboration LivePhilips Healthcare (Suzhou) Co., Ltd. · 2024
- Descendant · 3 generations on · 0 of its ownK241302 SonoSyncSamsung Medison Co., Ltd. · 2024
Most influential descendants
Showing 4 of 4 · See all- K201665Collaboration LivePhilips Ultrasound, Inc. · 2020 · cites it directly2descendants
- K212777Collaboration LivePhilips Ultrasound, Inc. · 2021 · 2 generations on1descendant
- K242329CT Collaboration LivePhilips Healthcare (Suzhou) Co., Ltd. · 2024 · cites it directly0descendants
- K241302SonoSyncSamsung Medison Co., Ltd. · 2024 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K971684 | Magnetom Project 047 System (Numaris 3.5 Software) | Siemens Medical Solutions USA, Inc. | 1997 | 4 |
| −5 | K032428 | Magnetom Avanto MR System | Siemens Medical Solutions USA, Inc. | 2003 | 4 |
| −4 | K041112 | Magnetom Espree System | Siemens Medical Solutions USA, Inc. | 2004 | 4 |
| −3 | K052423 | Magnetom Systems with Syngo Expert - I Option | Siemens Medi Cal Solutions, Inc. | 2006 | — |
| −2 | K061449 | Syngo Expert-1 | Siemens Medical Solution | 2006 | — |
| −1 | K150193 | Customer Remote Console (CRC) | Ge Medical Systems, LLC | 2015 | — |
| 0 (this device) | K200179 | Collaboration Live | Philips Health Care | 2020 | — |
| +1 | K201665 | Collaboration Live | Philips Ultrasound, Inc. | 2020 | — |
| +2 | K212777 | Collaboration Live | Philips Ultrasound, Inc. | 2021 | — |
| +1 | K242329 | CT Collaboration Live | Philips Healthcare (Suzhou) Co., Ltd. | 2024 | — |
| +3 | K241302 | SonoSync | Samsung Medison Co., Ltd. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1987 | 1 | 0 |
| 1991 | 1 | 0 |
| 1993 | 1 | 0 |
| 1994 | 1 | 0 |
| 1995 | 2 | 0 |
| 1996 | 2 | 0 |
| 1997 | 3 | 0 |
| 1999 | 1 | 0 |
| 2000 | 2 | 0 |
| 2001 | 3 | 0 |
| 2002 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 3 | 0 |
| 2008 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2024 | 2 | 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 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 K230955 syngo Application Softwarescore 21.5 · 11 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 |
|---|---|---|---|
| * | K150193 | Customer Remote Console (CRC)Summary page 5…e Predicate Device 510(k) GE Customer Remote Console K150193 4. Device Description Collaboration Live is a new software feature integrated in Philips Epiq and Affiniti Diagnostic Ul… | 2015 |
What descends from it? (4)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 23 years and passes through 5 companies; a new generation was cleared every 4.9 years on median.
- 13 of the 29 ancestors have a recall of any class.
- Of its descendants, K201665 (Philips Ultrasound, Inc., 2020) has gone furthest, with 2 descendants of its own.
- 3 other devices also cite its predicate K150193.
How does its category compare?
All LLZ devicesLLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · LLZ
58in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LLZ
173in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LLZ
11in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LLZ
116in 2025
MAUDE reports naming product code LLZ, 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 | 76 | 36 | 20 | 152 |
| 2008 | 94 | 52 | 32 | 154 |
| 2009 | 70 | 62 | 21 | 145 |
| 2010 | 51 | 98 | 17 | 145 |
| 2011 | 106 | 79 | 30 | 454 |
| 2012 | 82 | 87 | 12 | 266 |
| 2013 | 95 | 84 | 64 | 1,130 |
| 2014 | 78 | 89 | 6 | 15,631 |
| 2015 | 64 | 90 | 16 | 211 |
| 2016 | 82 | 90 | 12 | 290 |
| 2017 | 78 | 107 | 5 | 104 |
| 2018 | 104 | 105 | 7 | 72 |
| 2019 | 74 | 107 | 2 | 88 |
| 2020 | 81 | 115 | 6 | 82 |
| 2021 | 83 | 116 | 3 | 70 |
| 2022 | 65 | 137 | 4 | 28 |
| 2023 | 87 | 157 | 8 | 26 |
| 2024 | 62 | 131 | 6 | 42 |
| 2025 | 58 | 173 | 11 | 116 |
| 2026 | 45 | 110 | 14 | — |
What is it indicated for?
Collaboration Live is indicated for remote console access of the Philips ultrasound system for image viewing, image review, consultation, guidance, support, and education in real time. Access must be granted by the technologist operating the system. Images reviewed remotely are not for diagnostic use.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K200179 · printed Nov 5, 2026
Cite this page
510(k) Report. “K200179: Collaboration Live.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K200179
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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