510(k) Report

510(k) · Cleared

Recalled · Class II · 2022

Bantam

K091242510(k) TraditionalCleared Jul 6, 200969-day reviewClass II21 CFR 890.3110Recalls 1

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Altimate Medical, Inc. · INO Chair, Positioning, Electric

Cleared on Jul 6, 2009 as substantially equivalent to K062402 (Invacare Corp., 2006) after a 69-day review. Its family tree reaches back 2 generations to 1989. 1 later device descends from it. It has been recalled once.

Decided
Jul 6, 2009
Review
69 days
Class
Class II
Product code
INO
Recalls
1
Predicates
1

Its longest line of descent runs back 2 generations to K885343 (1989). 3 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor2013: 1 descendant clearedK885343 · Standex · Alt, Inc. · 1989K062402 · Easystand Evolv · Invacare Corp. · 20061990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 1 descendant K062402 · Easystand Evolv · Invacare Corp. · 2006K885343 · Standex · Alt, Inc. · 19890
  1. Root · 2 generations backK885343 StandexAlt, Inc. · 1989
  2. 1 generation backK062402 Easystand EvolvInvacare Corp. · 2006
  3. This deviceK091242 BantamAltimate Medical, Inc. · 2009
  4. Descendant · cites it directly · 0 of its ownK123834 Easystand Bantam MediumAltimate Medical, Inc. · 2013

Most influential descendants

Showing 1 of 1 · See all
  • K123834Easystand Bantam MediumAltimate Medical, Inc. · 2013 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K885343StandexAlt, Inc.1989—
−1K062402Easystand EvolvInvacare Corp.2006—
0 (this device)K091242BantamAltimate Medical, Inc.2009—
+1K123834Easystand Bantam MediumAltimate Medical, Inc.2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
FIG. 1 — Lineage of K091242, 1989–2013Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

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
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K062402Easystand Evolv
Summary page 1
…ame: Electric lift chair Classification Name: Chair, positioning, electric per 21 CFR 890.3110 K062402 Legally Marketed Predicate Device(s): Altimate Medical EasyStand Evolv; September 21, 200…
Invacare Corp.2006—

Also cleared against K062402: 1 other device →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K123834Easystand Bantam MediumAltimate Medical, Inc.20130

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Oct 4, 2022Class IIZ-0243-2023PendingSome EasyStand Bantam Small and Extra Small standers with the non-supine option may have been manufactured with a component that affects the operation of the leg assembly bracket to maintain the standers non-supine position.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 20 years and passes through 3 companies; a new generation was cleared every 17.4 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K123834 (Altimate Medical, Inc., 2013) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K062402.

How does its category compare?

All INO devices

INO Chair, Positioning, Electric: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · INO

1in 2014

2007: 22008: 22009: 42010: 12011: 12013: 12014: 1
2007high 4 (2009) · low 0 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · INO

126in 2009

2009: 126 days median
2007high 126 (2009)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · INO

1in 2022

2022: 1
2007high 1 (2022) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · INO

29in 2025

2007: 12008: 52009: 62010: 72011: 202012: 152013: 242014: 162015: 232016: 352017: 382018: 382019: 372020: 412021: 492022: 292023: 292024: 202025: 29
2007high 49 (2021) · low 1 (2007)2025

MAUDE reports naming product code INO, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—01
20082—05
2009412606
20101—07
20111—020
20120—015
20131—024
20141—016
20150—023
20160—035
20170—038
20180—038
20190—037
20200—041
20210—049
20220—129
20230—029
20240—020
20250—029
20260—0—

What is it indicated for?

The Altimate Medical EasyStand Bantam is intended to assist persons who have difficulty rising from a seated position to a standing position and is indicated for persons weighing between 50 - 100 lbs., including pediatrics.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K091242: Bantam.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K091242

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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