510(k) · Cleared
ClearedHausted Powertran Series Stretcher
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
STERIS Corporation · INK Stretcher, Wheeled, Powered
Cleared on Sep 9, 2004 after a 55-day review. The FDA summary names its predicate without a number. 12 later devices descend from it.
- Decided
- Sep 9, 2004
- Review
- 55 days
- Class
- Class II
- Product code
- INK
- Recalls
- None
- Predicates
- 0
12 later devices descend from it, 1 citing it directly.
- This deviceK041924 Hausted Powertran Series StretcherSTERIS Corporation · 2004
- Descendant · cites it directly · 11 of its ownK090136 Steris Cmax XLT Surgical TableSTERIS Corporation · 2009 · Recalled
- Descendant · 2 generations on · 10 of its ownK112109 The Kinegraph Vma Software, the Motion Normalizer Patient Handling…Ortho Kinematics, Inc. · 2011
- Descendant · 2 generations on · 9 of its ownK130743 The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.0…Ortho Kinematics, Inc. · 2013
- Descendant · 3 generations on · 8 of its ownK133875 The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.2…Ortho Kinematics, Inc. · 2014 · Recalled
- Descendant · 4 generations on · 7 of its ownK172327 VMA™ System version 3.0Ortho Kinematics, Inc. · 2017
Showing 5 of 12 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 12 · See all- K090136Steris Cmax XLT Surgical TableSTERIS Corporation · 2009 · cites it directly11descendants
- K112109The Kinegraph Vma Software, the Motion Normalizer Patient Handling and Data Collection…Ortho Kinematics, Inc. · 2011 · 2 generations on10descendants
- K130743The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.0; the Motion…Ortho Kinematics, Inc. · 2013 · 2 generations on9descendants
- K133875The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.2, the Motion…Ortho Kinematics, Inc. · 2014 · 3 generations on8descendants
- K172327VMA™ System version 3.0Ortho Kinematics, Inc. · 2017 · 4 generations on7descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K041924 | Hausted Powertran Series Stretcher | STERIS Corporation | 2004 | — |
| +1 | K090136 | Steris Cmax XLT Surgical Table | STERIS Corporation | 2009 | 4 |
| +2 | K112109 | The Kinegraph Vma Software, the Motion Normalizer Patient Handling and Data… | Ortho Kinematics, Inc. | 2011 | — |
| +2 | K130743 | The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.0; the Motion… | Ortho Kinematics, Inc. | 2013 | — |
| +3 | K133875 | The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.2, the Motion… | Ortho Kinematics, Inc. | 2014 | 4 |
| +4 | K172327 | VMA™ System version 3.0 | Ortho Kinematics, Inc. | 2017 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
| 2011 | 1 | 0 |
| 2013 | 1 | 0 |
| 2014 | 1 | 0 |
| 2017 | 1 | 0 |
| 2019 | 1 | 0 |
| 2021 | 1 | 0 |
| 2023 | 2 | 0 |
| 2025 | 2 | 0 |
| 2026 | 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 INK? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin 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 |
|---|---|---|---|
| * | — | Stryker ZOOM® Motorized Stretchers Named without a submission number | |
| * | — | Stryker Powered Wheeled Stretcher Named without a submission number |
What descends from it? (12)
See all 121 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K090136 | Steris Cmax XLT Surgical Table | 2009 | 11 |
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?
- Of its descendants, K090136 (STERIS Corporation, 2009) has gone furthest, with 11 descendants of its own.
How does its category compare?
All INK devicesINK Stretcher, Wheeled, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · INK
1in 2016
2026 to Oct 25, outlined.
Median 510(k) review, days · INK
Too few INK 510(k)s in any year since 2007 to give a median.
Recalls per year · INK
7in 2011
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · INK
101in 2025
MAUDE reports naming product code INK, 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 | 0 | — | 0 | 13 |
| 2008 | 0 | — | 0 | 6 |
| 2009 | 1 | — | 0 | 81 |
| 2010 | 1 | — | 5 | 529 |
| 2011 | 2 | — | 7 | 1,529 |
| 2012 | 0 | — | 0 | 625 |
| 2013 | 0 | — | 0 | 438 |
| 2014 | 1 | — | 0 | 88 |
| 2015 | 0 | — | 0 | 4 |
| 2016 | 1 | — | 0 | 5 |
| 2017 | 0 | — | 0 | 5 |
| 2018 | 0 | — | 0 | 63 |
| 2019 | 0 | — | 0 | 79 |
| 2020 | 0 | — | 0 | 89 |
| 2021 | 0 | — | 0 | 114 |
| 2022 | 0 | — | 0 | 93 |
| 2023 | 0 | — | 0 | 147 |
| 2024 | 0 | — | 0 | 179 |
| 2025 | 0 | — | 0 | 101 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Hausted® POWERTRAN T M Series Stretcher is a powered patient transport. This device is a motorized device intended for medical purposes to assist in the transfer of patients to and from the bath, beds, chairs, treatment modalities, and transport vehicles. The FDA has classified powered patient transports as a Class II device.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K041924 · printed Nov 6, 2026
Cite this page
510(k) Report. “K041924: Hausted Powertran Series Stretcher.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K041924
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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