510(k) · Cleared
ClearedEasystand Bantam Medium
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Altimate Medical, Inc. · INO Chair, Positioning, Electric
Cleared on Aug 13, 2013 as substantially equivalent to K091242 (Altimate Medical, Inc., 2009) after a 243-day review. Its family tree reaches back 3 generations to 1989.
- Decided
- Aug 13, 2013
- Review
- 243 days
- Class
- Class II
- Product code
- INO
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K885343 (1989). 4 ancestors in all. No later device cites it as a predicate yet.
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K885343 | Standex | Alt, Inc. | 1989 | — |
| −2 | K062402 | Easystand Evolv | Invacare Corp. | 2006 | — |
| −1 | K091242 | Bantam | Altimate Medical, Inc. | 2009 | 1 |
| 0 (this device) | K123834 | Easystand Bantam Medium | Altimate Medical, Inc. | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 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 INO? 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? (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 |
|---|---|---|---|
| * | K091242 | BantamSummary page 1…ame: Electric Lift Chair Classification Name: Chair, positioning, electric per 21 CFR 890.3110 Legally Marketed Predicate Device(s): Altimate Medical EasyStand Bantam: K09 1242 July 6, 2009 INVACARE CORPORATION… | 2009 |
What descends from it?
No later submission names this one as a predicate yet.
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 24 years and passes through 3 companies; a new generation was cleared every 4.1 years on median.
- 1 of the 4 ancestors has a recall of any class.
How does its category compare?
All INO devicesINO Chair, Positioning, Electric: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · INO
1in 2014
2026 to Oct 25, outlined.
Median 510(k) review, days · INO
126in 2009
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · INO
1in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · INO
29in 2025
MAUDE reports naming product code INO, 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 | 2 | — | 0 | 1 |
| 2008 | 2 | — | 0 | 5 |
| 2009 | 4 | 126 | 0 | 6 |
| 2010 | 1 | — | 0 | 7 |
| 2011 | 1 | — | 0 | 20 |
| 2012 | 0 | — | 0 | 15 |
| 2013 | 1 | — | 0 | 24 |
| 2014 | 1 | — | 0 | 16 |
| 2015 | 0 | — | 0 | 23 |
| 2016 | 0 | — | 0 | 35 |
| 2017 | 0 | — | 0 | 38 |
| 2018 | 0 | — | 0 | 38 |
| 2019 | 0 | — | 0 | 37 |
| 2020 | 0 | — | 0 | 41 |
| 2021 | 0 | — | 0 | 49 |
| 2022 | 0 | — | 1 | 29 |
| 2023 | 0 | — | 0 | 29 |
| 2024 | 0 | — | 0 | 20 |
| 2025 | 0 | — | 0 | 29 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Altimate Medical EasyStand Bantam Medium is intended to assist persons who have difficulty rising from a seated position to a standing position and is indicated for persons weighing up to 200lbs.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K123834 · printed Nov 6, 2026
Cite this page
510(k) Report. “K123834: Easystand Bantam Medium.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123834
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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