510(k) · Cleared
ClearedInsight Plus 9000 Phased Array Torso and Plevis Coil
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Usa Instruments, Inc. · MOS Coil, Magnetic Resonance, Specialty
Cleared on Jan 24, 2003 as substantially equivalent to K001209 (Usa Instruments, Inc., 2000) and 1 other predicate after an 86-day review. Its family tree reaches back 1 generation to 2000. 2 later devices descend from it.
- Decided
- Jan 24, 2003
- Review
- 86 days
- Class
- Class II
- Product code
- MOS
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K001209 (2000). 2 ancestors in all. 2 later devices descend from it, 1 citing it directly.
- Root · 1 generation backK001209 Insight Plus 9000 Phased Array Torso and Pelvis CoilUsa Instruments, Inc. · 2000
- This deviceK023650 Insight Plus 9000 Phased Array Torso and Plevis CoilUsa Instruments, Inc. · 2003
- Descendant · cites it directly · 1 of its ownK031172 Spirit Iii Totalsense Cardiac CoilUsa Instruments, Inc. · 2003
- Descendant · 2 generations on · 0 of its ownK033490 Spirit 5000 Cardiac CoilUsa Instruments, Inc. · 2004
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K001209 | Insight Plus 9000 Phased Array Torso and Pelvis Coil | Usa Instruments, Inc. | 2000 | — |
| 0 (this device) | K023650 | Insight Plus 9000 Phased Array Torso and Plevis Coil | Usa Instruments, Inc. | 2003 | — |
| +1 | K031172 | Spirit Iii Totalsense Cardiac Coil | Usa Instruments, Inc. | 2003 | — |
| +2 | K033490 | Spirit 5000 Cardiac Coil | Usa Instruments, Inc. | 2004 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2003 | 1 | 0 |
| 2004 | 1 | 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 MOS? 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 MOS device
- #1 K253738 3.0T Air 32CH Hnascore 15.2 · 16 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K001209 | Insight Plus 9000 Phased Array Torso and Pelvis CoilSummary page 2…ased Array Torso coil. and Pelvis Coil manufactured by USA Instruments, Inc. (K001209) -Similar to the Flow 7000 Peripheral Vascular Coil… | 2000 |
| * | K010730 | Modification to Flow 7000 Peripheral Vascular CoilSummary page 2…-Similar to the Flow 7000 Peripheral Vascular Coil manufactured by USA Instruments, Inc. (K010730) Prevention of RF Burns: Does not transmit -Similar to the Insight Plus 9000 Phased Array Torso RF power; decoupling isol… | 2001 |
| † | K013854 | Mark 5000 Quadrature Shoulder Coil | 2002 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K031172 | Spirit Iii Totalsense Cardiac Coil | 2003 | 1 |
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?
How does its category compare?
All MOS devicesMOS Coil, Magnetic Resonance, Specialty: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · MOS
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MOS
59in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MOS
13in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MOS
2in 2025
MAUDE reports naming product code MOS, 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 | 16 | 19 | 0 | 4 |
| 2008 | 19 | 33 | 2 | 2 |
| 2009 | 10 | 43 | 0 | 5 |
| 2010 | 16 | 78 | 1 | 13 |
| 2011 | 25 | 57 | 0 | 7 |
| 2012 | 15 | 49 | 1 | 12 |
| 2013 | 7 | 87 | 0 | 10 |
| 2014 | 12 | 60 | 0 | 4 |
| 2015 | 6 | 58 | 2 | 5 |
| 2016 | 11 | 42 | 0 | 7 |
| 2017 | 9 | 63 | 0 | 9 |
| 2018 | 10 | 30 | 0 | 7 |
| 2019 | 3 | 178 | 8 | 8 |
| 2020 | 5 | 51 | 1 | 2 |
| 2021 | 4 | 41 | 0 | 3 |
| 2022 | 11 | 79 | 0 | 5 |
| 2023 | 10 | 59 | 0 | 4 |
| 2024 | 10 | 39 | 13 | 8 |
| 2025 | 3 | 59 | 0 | 2 |
| 2026 | 10 | 45 | 0 | — |
What is it indicated for?
The Insight Plus 9000 Phased Array Torso and Pelvis Coil is designed to provide Magnetic Resonance Images of the torso and pelvic regions, including the abdomen, chest, and hips. The Insight Plus 9000 Phased Array Torso and Pelvis Coil is designed for use with the Philips lntera 1.5T MRI scanner manufactured by Philips Medical Systems, lnc. Anatomic Regions: Torso and pelvic regions, including the abdomen, chest, and hips. Nuclei Excited: Hydrogen The…
Read the full statement (159 words)
The Insight Plus 9000 Phased Array Torso and Pelvis Coil is designed to provide Magnetic Resonance Images of the torso and pelvic regions, including the abdomen, chest, and hips. The Insight Plus 9000 Phased Array Torso and Pelvis Coil is designed for use with the Philips lntera 1.5T MRI scanner manufactured by Philips Medical Systems, lnc.
Anatomic Regions: Torso and pelvic regions, including the abdomen, chest, and hips.
Nuclei Excited: Hydrogen
The indications for use are the same as for standard imaging:
The 1.5T MRI system is indicated for use as an NMR device that produces images that: (1) correspond to the distribution of protons exhibiting NMR signal, (2) depend upon NMR parameters (proton density, spin lattice relaxation time T I , spin-spin relaxation time T2) and (3) display the soft tissue structure of the head and whole body. When interpreted by a trained physician, these images yield information that can be useful in the determination of a diagnosis.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K023650 · printed Nov 6, 2026
Cite this page
510(k) Report. “K023650: Insight Plus 9000 Phased Array Torso and Plevis Coil.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K023650
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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