510(k) Report

510(k) · Cleared

Cleared

Transport Series Transport Chair

K050281510(k) TraditionalCleared Apr 11, 200563-day reviewClass I21 CFR 890.3850

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

Access Point Medical, LLC · IOR Wheelchair, Mechanical

Cleared on Apr 11, 2005 as substantially equivalent to K002673 (Jiangsu Intco Medical Equipment & Supply Co., Ltd., 2000) after a 63-day review. Its family tree reaches back 1 generation to 2000.

Decided
Apr 11, 2005
Review
63 days
Class
Class I
Product code
IOR
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K002673 (2000). No later device cites it as a predicate yet.

  1. Root · 1 generation backK002673 EZ-Comfort Transporter 2000 SeriesJiangsu Intco Medical Equipment & Supply Co., Ltd. · 2000
  2. This deviceK050281 Transport Series Transport ChairAccess Point Medical, LLC · 2005
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K002673EZ-Comfort Transporter 2000 SeriesJiangsu Intco Medical Equipment & Supply Co., Ltd.2000—
0 (this device)K050281Transport Series Transport ChairAccess Point Medical, LLC2005—
FIG. 1 — Lineage of K050281, 2000–2005Source: 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 IOR? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new IOR device

  1. #1 K201461 Manual Wheelchair, Model A011score 20.0 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin 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
*K002673EZ-Comfort Transporter 2000 Series
Summary page 2
…ersons limited to a sitting position N. PREDICATE DEVICE Jiangsu Intco Medical Equipment & Supply Co., Ltd. EZ-Comfort Transporter 2000 series (K002673). 0. COMPARISON OF TECHNOLOGICAL CHARACTERISTICS: The AXS Transport Chair and the Jiangsu Intco Medical Equipment & S…
Jiangsu Intco Medical Equipment & Supply Co., Ltd.2000—

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.

How does its category compare?

All IOR devices

IOR Wheelchair, Mechanical: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · IOR

17so far in 2026, the most since 2007

2007: 52008: 132009: 42010: 122011: 62012: 112013: 72014: 72015: 32016: 102017: 72018: 32019: 62020: 22021: 22022: 42023: 92024: 42025: 72026 (partial year): 17
2007high 17 (2026) · low 2 (2020)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IOR

91in 2025

2007: 38 days median2008: 32 days median2009: 43 days median2010: 81 days median2011: 58 days median2012: 176 days median2013: 233 days median2014: 211 days median2015: 104 days median2016: 135 days median2017: 209 days median2018: 203 days median2019: 160 days median2022: 150 days median2023: 61 days median2024: 65 days median2025: 91 days median2026 (partial year): 103 days median
2007high 233 (2013) · low 32 (2008)2026

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

Recalls per year · IOR

1in 2021

2007: 12008: 32009: 22011: 62012: 32013: 32014: 32016: 12021: 1
2007high 6 (2011) · low 0 (2010)2026

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

Adverse event reports per year · IOR

135in 2025

2007: 362008: 622009: 542010: 692011: 2322012: 1,2382013: 4,6742014: 5,0822015: 4,4722016: 1,8602017: 492018: 582019: 532020: 432021: 592022: 372023: 1652024: 1382025: 135
2007high 5,082 (2014) · low 36 (2007)2025

MAUDE reports naming product code IOR, 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
2007538136
20081332362
2009443254
20101281069
20116586232
20121117631,238
2013723334,674
2014721135,082
2015310404,472
20161013511,860
20177209049
20183203058
20196160053
20202—043
20212—159
20224150037
20239610165
20244650138
20257910135
2026171030—

What is it indicated for?

AXS Transport Chairs are indicated for providing mobility to persons limited to a sitting position

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K050281: Transport Series Transport Chair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K050281

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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