510(k) · Cleared
ClearedBruno Electra-Ride Stairway Elevator System. Model Sre-1540
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Bruno Independent Living Aids, Inc. · ILK Transport, Patient, Powered
Cleared on Dec 12, 2003 after an 11-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 2 later devices descend from it.
- Decided
- Dec 12, 2003
- Review
- 11 days
- Class
- Class II
- Product code
- ILK
- Recalls
- None
- Predicates
- 0
2 later devices descend from it, 2 citing it directly.
- This deviceK033752 Bruno Electra-Ride Stairway Elevator System. Model Sre-1540Bruno Independent Living Aids, Inc. · 2003
- Descendant · cites it directly · 0 of its ownK091858 Pinnacle Stair Way LiftSummit Harmar, LLC · 2009
- Descendant · cites it directly · 0 of its ownK073110 Merits E600 Series Stair LiftMerits Health Products Co., Ltd. · 2008
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 |
|---|---|---|---|---|---|
| 0 (this device) | K033752 | Bruno Electra-Ride Stairway Elevator System. Model Sre-1540 | Bruno Independent Living Aids, Inc. | 2003 | — |
| +1 | K091858 | Pinnacle Stair Way Lift | Summit Harmar, LLC | 2009 | — |
| +1 | K073110 | Merits E600 Series Stair Lift | Merits Health Products Co., Ltd. | 2008 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2008 | 1 | 0 |
| 2009 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in ILK? 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 ILK device
- #1 K222818 Xpedition ™ Powered Stair Chair (625700000000)score 5.3 · 3 generations · no Class I recall
What was it cleared against?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (2)
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?
- Of its descendants, K091858 (Summit Harmar, LLC, 2009) has gone furthest, with 0 descendants of its own.
How does its category compare?
All ILK devicesILK Transport, Patient, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · ILK
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · ILK
150in 2012
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · ILK
1in 2012
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · ILK
32in 2025
MAUDE reports naming product code ILK, 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 | 1 |
| 2008 | 1 | — | 0 | 4 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 2 | — | 0 | 1 |
| 2011 | 1 | — | 0 | 1 |
| 2012 | 3 | 150 | 1 | 4 |
| 2013 | 0 | — | 0 | 4 |
| 2014 | 1 | — | 0 | 2 |
| 2015 | 0 | — | 0 | 2 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 1 | — | 0 | 5 |
| 2024 | 1 | — | 0 | 18 |
| 2025 | 0 | — | 0 | 32 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Bruno Electra-Ride TM, Model Sre-1540 and Electra-Ride TM II, Model SRE-1550, is a Powered Patient Transport, also commonly known as a Stairway Chairlift, or Stairlift. It is a motorized device intended for medical purposes to assist transfers of patients, or mobility-impaired persons, up and down flights of stairs.
Indications for use as stated in the FDA 510(k) statement.
https://510kreport.com/device/K033752 · printed Nov 3, 2026
Cite this page
510(k) Report. “K033752: Bruno Electra-Ride Stairway Elevator System. Model Sre-1540.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K033752
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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