510(k) Report

510(k) · Cleared

Cleared

V-1504 Vertical Platform Lift

K960739510(k) TraditionalCleared Apr 1, 199638-day reviewClass II21 CFR 890.3930

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

Barnes,Richardson & Colburn · ING Elevator, Wheelchair, Portable

Cleared on Apr 1, 1996 as substantially equivalent to K934553 (The National Wheel-O-Vator Co., Inc., 1994) after a 38-day review. Its family tree reaches back 1 generation to 1994. 3 later devices descend from it.

Decided
Apr 1, 1996
Review
38 days
Class
Class II
Product code
ING
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K934553 (1994). 3 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared2003: 1 descendant cleared2012: 1 descendant clearedK934553 · Wheel-O-Vator · The National Wheel-O-Vator Co., Inc. · 19941990200020102020
Descendants, by generation 1 generation forward: 3 descendants K934553 · Wheel-O-Vator · The National Wheel-O-Vator Co., Inc. · 19940
  1. Root · 1 generation backK934553 Wheel-O-VatorThe National Wheel-O-Vator Co., Inc. · 1994
  2. This deviceK960739 V-1504 Vertical Platform LiftBarnes,Richardson & Colburn · 1996
  3. Descendant · cites it directly · 1 of its ownK033469 Genesis Vertical Platform LiftGaraventa Accessibility · 2004
  4. Descendant · cites it directly · 0 of its ownK113065 RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012
  5. Descendant · cites it directly · 0 of its ownK024346 The MultiliftServices Industriels Savaria, Inc. · 2003

Most influential descendants

Showing 3 of 3 · See all
  • K033469Genesis Vertical Platform LiftGaraventa Accessibility · 2004 · cites it directly1descendant
  • K113065RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012 · cites it directly0descendants
  • K024346The MultiliftServices Industriels Savaria, Inc. · 2003 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K934553Wheel-O-VatorThe National Wheel-O-Vator Co., Inc.1994—
0 (this device)K960739V-1504 Vertical Platform LiftBarnes,Richardson & Colburn1996—
+1K033469Genesis Vertical Platform LiftGaraventa Accessibility2004—
+1K113065RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC2012—
+1K024346The MultiliftServices Industriels Savaria, Inc.2003—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
200410
201210
FIG. 1 — Lineage of K960739, 1994–2012Source: 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 ING? 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
*K934553Wheel-O-Vator
Summary page 1
…5 Contact: Ansis M. Helmanis Tel: (202) 457-0300 February 9, 1996 Savaria V-1504 Vertical Platform Lift The National Wheel-O-Vator Co., Inc. Vertical Wheelchair Lift (K934553). See ATTACHMENT B for product literature. The V-1504 Vertical Platform Lift is a a lift designed to carry a maximum of one whee…
The National Wheel-O-Vator Co., Inc.1994—

What descends from it? (3)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K033469Genesis Vertical Platform LiftGaraventa Accessibility20041
K113065RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC20120
K024346The MultiliftServices Industriels Savaria, Inc.20030

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?

  • Its one ancestor has no recall.
  • Of its descendants, K033469 (Garaventa Accessibility, 2004) has gone furthest, with 1 descendant of its own.

How does its category compare?

All ING devices

ING Elevator, Wheelchair, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · ING

1in 2012

2008: 12009: 22010: 12011: 12012: 1
2007high 2 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ING

Too few ING 510(k)s in any year since 2007 to give a median.

Recalls per year · ING

3in 2007

2007: 3
2007high 3 (2007) · low 0 (2008)2026

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

Adverse event reports per year · ING

4in 2024

2010: 12012: 12017: 22018: 72019: 42020: 72021: 62022: 32023: 22024: 4
2007high 7 (2018) · low 0 (2007)2025

MAUDE reports naming product code ING, 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
20070—30
20081—00
20092—00
20101—01
20111—00
20121—01
20130—00
20140—00
20150—00
20160—00
20170—02
20180—07
20190—04
20200—07
20210—06
20220—03
20230—02
20240—04
20250—00
20260—0—

What is it indicated for?

The V-1504 Vertical Platform Lift is intended to mechanically transport an individual in a wheelchair directly between floors in a private residence or public facility.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K960739: V-1504 Vertical Platform Lift.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K960739

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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