510(k) Report

510(k) · Cleared

Cleared

Dalton Lift Chair

K131909510(k) TraditionalCleared Feb 24, 2014243-day reviewClass II21 CFR 890.3110

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

Dalton Instrument Corp. · INO Chair, Positioning, Electric

Cleared on Feb 24, 2014 as substantially equivalent to K070950 (Pride Mobility Products Corp., 2007) after a 243-day review. Its family tree reaches back 2 generations to 1995.

Decided
Feb 24, 2014
Review
243 days
Class
Class II
Product code
INO
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K953342 (1995). No later device cites it as a predicate yet.

  1. Root · 2 generations backK953342 TMR48Pride Health Care, Inc. · 1995 · Recalled
  2. 1 generation backK070950 Lift Chair, Model C5Pride Mobility Products Corp. · 2007
  3. This deviceK131909 Dalton Lift ChairDalton Instrument Corp. · 2014
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K953342TMR48Pride Health Care, Inc.19951
−1K070950Lift Chair, Model C5Pride Mobility Products Corp.2007—
0 (this device)K131909Dalton Lift ChairDalton Instrument Corp.2014—
FIG. 1 — Lineage of K131909, 1995–2014Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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
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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
*K070950Lift Chair, Model C5
Summary page 1
…proposed 'Dalton Lift Chair, L-C-1 06' is substantially equivalent to the Lift Chair Model C5 manufactured by Pride Mobility Products Corp., previously cleared under K070950. 5-1 4. Description of Device The Dalton Lift Chair,…
Pride Mobility Products Corp.2007—

Also cleared against K070950: 1 other device →

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 19 years and passes through 3 companies; a new generation was cleared every 11.6 years on median.
  • 1 of the 2 ancestors has a recall of any class.
  • 1 other device also cites its predicate K070950.

How does its category compare?

All INO devices

INO Chair, Positioning, Electric: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, 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 intended use of the Dalton Lift Chair, Model LC-106 is to provide lift assistance for persons who have difficulty rising from a seated position to a standing position.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K131909: Dalton Lift Chair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K131909

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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