510(k) Report

510(k) · Cleared

Cleared

Liftkar PT

K110495510(k) TraditionalCleared May 20, 201187-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

Sano Transportgerate GmbH · ING Elevator, Wheelchair, Portable

Cleared on May 20, 2011 as substantially equivalent to K920105 (Alber Technologies, Inc., 1992) after an 87-day review. Its family tree reaches back 1 generation to 1992.

Decided
May 20, 2011
Review
87 days
Class
Class II
Product code
ING
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K920105 (1992). No later device cites it as a predicate yet.

K920105 · Scalamobil · Alber Technologies, Inc. · 199219901995200020052010
K920105 · Scalamobil · Alber Technologies, Inc. · 19920
  1. Root · 1 generation backK920105 ScalamobilAlber Technologies, Inc. · 1992
  2. This deviceK110495 Liftkar PTSano Transportgerate GmbH · 2011
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K920105ScalamobilAlber Technologies, Inc.1992—
0 (this device)K110495Liftkar PTSano Transportgerate GmbH2011—
FIG. 1 — Lineage of K110495, 1992–2011Source: 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
*K920105Scalamobil
Summary page 1
…PTr Product of SANO Common Name Elevator, Wheelchair Classification Name Class 11 General Controls and Special Controls. Elevator Wheelchair Predicate Device Scalamobil (K920105) Intended Use The intended use of the LIFTKAR PrT " is to transport a wheelchair user or a person needing assistance up or down s…
Alber Technologies, Inc.1992—

Also cleared against K920105: 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?

  • Its one ancestor has no recall.
  • 1 other device also cites its predicate K920105.

How does its category compare?

All ING devices

ING Elevator, Wheelchair, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

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 LIFTKAR PT'M Is a wheelchair, elevator commonly known as an easy method of transporting wheelchair users or disabled persons, up and down stairs safely. This is done with a lifting mechanism. it is a battery powered attendant operated mobile stair-climber. LIFTKAR PT' can be used on any stairs indoors or outside.

Indications for use as stated in the FDA summary.

Also cleared against K920105

1 other device cites the same predicate.

  • K103122C-Max, C-Max U1, C-Max U1 160KG, C-Max U2, C-Max U2 160KG, S-Max, S-Max Aviation, S-Max Sella, S-Max Sella…Aat Alber Antriebstechnik GmbH · 2010

Recent decisions in ING

The ING category page

  • K113065RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012
  • K102088Journey Inclined Platform Lift and Supra Curved Incline Platform LiftThyssenkrupp Ceteco Srl · 2010
  • K091881RPL/CPL Vertical Platform LiftsHarmar Summit, LLC · 2009
  • K090856Journey (or RPSP), Journey Cubic (or Supra or TP02)Thyssenkrupp Ceteco Srl · 2009
  • K073513Merits E700 Porce LiftMerits Health Products Co., Ltd. · 2008

https://510kreport.com/device/K110495 · printed Nov 6, 2026

Cite this page

510(k) Report. “K110495: Liftkar PT.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110495

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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