510(k) · Cleared
Recalled · 2003Philips Integris V3000 Rotational Angio Function
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Philips Medical Systems, Inc. · IZI System, X-Ray, Angiographic
Cleared on Oct 16, 1992 after a 79-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it. It has been recalled once.
- Decided
- Oct 16, 1992
- Review
- 79 days
- Class
- Class II
- Product code
- IZI
- Recalls
- 1
- Predicates
- 0
4 later devices descend from it, 3 citing it directly.
- This deviceK923813 Philips Integris V3000 Rotational Angio FunctionPhilips Medical Systems, Inc. · 1992
- Descendant · cites it directly · 1 of its ownK964990 Hitachi SX-VA30 C-Arm Fluoroscopic/Angiographic System (SX-VA30)Hitachi Medical Systems America, Inc. · 1997
- Descendant · 2 generations on · 0 of its ownK991231 Hitachi VersiflexHitachi Medical Systems America, Inc. · 1999
- Descendant · cites it directly · 0 of its ownK990055 B-400 Ceiling Mounted Possitioner, Model B-400Omega Medical Imaging, Inc. · 1999
- Descendant · cites it directly · 0 of its ownK971489 Ratational Angiography Option for Philips Multidiagnost 4Philips Medical Systems North America, Inc. · 1997
Most influential descendants
Showing 4 of 4 · See all- K964990Hitachi SX-VA30 C-Arm Fluoroscopic/Angiographic System (SX-VA30)Hitachi Medical Systems America, Inc. · 1997 · cites it directly1descendant
- K991231Hitachi VersiflexHitachi Medical Systems America, Inc. · 1999 · 2 generations on0descendants
- K990055B-400 Ceiling Mounted Possitioner, Model B-400Omega Medical Imaging, Inc. · 1999 · cites it directly0descendants
- K971489Ratational Angiography Option for Philips Multidiagnost 4Philips Medical Systems North America, Inc. · 1997 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K923813 | Philips Integris V3000 Rotational Angio Function | Philips Medical Systems, Inc. | 1992 | — |
| +1 | K964990 | Hitachi SX-VA30 C-Arm Fluoroscopic/Angiographic System (SX-VA30) | Hitachi Medical Systems America, Inc. | 1997 | — |
| +2 | K991231 | Hitachi Versiflex | Hitachi Medical Systems America, Inc. | 1999 | — |
| +1 | K990055 | B-400 Ceiling Mounted Possitioner, Model B-400 | Omega Medical Imaging, Inc. | 1999 | — |
| +1 | K971489 | Ratational Angiography Option for Philips Multidiagnost 4 | Philips Medical Systems North America, Inc. | 1997 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 2 | 0 |
| 1999 | 2 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in IZI? 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 IZI device
- #1 K230727 SPY Portable Handheld Imaging (SPY-PHI) Systemscore 23.2 · 20 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (4)
3 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)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Oct 10, 2003 | Not classified | Z-0097-04 | Other | The thumbscrew hinge pin on the monitor support arm could become loose allowing the monitor to fall. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K964990 (Hitachi Medical Systems America, Inc., 1997) has gone furthest, with 1 descendant of its own.
How does its category compare?
All IZI devicesIZI System, X-Ray, Angiographic: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · IZI
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IZI
81in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IZI
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IZI
2,171in 2025
MAUDE reports naming product code IZI, 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 | 7 | 28 | 6 | 92 |
| 2008 | 6 | 68 | 52 | 101 |
| 2009 | 2 | — | 18 | 132 |
| 2010 | 2 | — | 11 | 252 |
| 2011 | 4 | 104 | 6 | 377 |
| 2012 | 1 | — | 6 | 77 |
| 2013 | 1 | — | 6 | 58 |
| 2014 | 4 | 111 | 5 | 123 |
| 2015 | 0 | — | 14 | 36 |
| 2016 | 1 | — | 7 | 102 |
| 2017 | 2 | — | 1 | 88 |
| 2018 | 2 | — | 2 | 49 |
| 2019 | 2 | — | 2 | 30 |
| 2020 | 1 | — | 2 | 14 |
| 2021 | 1 | — | 1 | 29 |
| 2022 | 1 | — | 0 | 265 |
| 2023 | 3 | 81 | 0 | 1,204 |
| 2024 | 2 | — | 0 | 1,332 |
| 2025 | 2 | — | 0 | 2,171 |
| 2026 | 2 | — | 1 | — |
https://510kreport.com/device/K923813 · printed Nov 6, 2026
Cite this page
510(k) Report. “K923813: Philips Integris V3000 Rotational Angio Function.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K923813
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026