510(k) Report

510(k) · Cleared

Cleared

Heartway Attendant-Controlled Power Chair, TC1

K071006510(k) TraditionalCleared May 21, 200742-day reviewClass II21 CFR 890.3860

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

Heartway Medical Products Co., Ltd. · ITI Wheelchair, Powered

Cleared on May 21, 2007 as substantially equivalent to K070489 (Heartway Medical Products Co., Ltd., 2007) after a 42-day review. Its family tree reaches back 3 generations to 2003. 5 later devices descend from it.

Decided
May 21, 2007
Review
42 days
Class
Class II
Product code
ITI
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K022697 (2003). 5 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2010: 1 descendant cleared2011: 1 descendant cleared2012: 1 descendant cleared2014: 2 descendants clearedK022697 · Teh Lin Jupiter Power Chair, Model TL-320 · Teh Lin Prosthetic & Orthopaedic, Inc. · 2003K061693 · Foryou Powered Wheelchair, Model FC-100 · Foryou Technology Co., Ltd. · 2006K070489 · Heartway Power Tilt Seating System Power Chair, Model# P16RT · Heartway Medical Products Co., Ltd. · 2007200020052010201520202025
  1. Root · 3 generations backK022697 Teh Lin Jupiter Power Chair, Model TL-320Teh Lin Prosthetic & Orthopaedic, Inc. · 2003
  2. 2 generations backK061693 Foryou Powered Wheelchair, Model FC-100Foryou Technology Co., Ltd. · 2006
  3. 1 generation backK070489 Heartway Power Tilt Seating System Power Chair, Model# P16RTHeartway Medical Products Co., Ltd. · 2007
  4. This deviceK071006 Heartway Attendant-Controlled Power Chair, TC1Heartway Medical Products Co., Ltd. · 2007
  5. Descendant · cites it directly · 1 of its ownK111095 Breeze Electric Transport Chair Model 1025Electro Kinetic Technologies, LLC · 2011
  6. Descendant · cites it directly · 1 of its ownK100327 Heartway Power Chair, P23Heartway Medical Products Co., Ltd. · 2010
  7. Descendant · 2 generations on · 0 of its ownK132856 Heartway Power WheelchairHeartway Medical Products Co., Ltd. · 2014
  8. Descendant · 2 generations on · 0 of its ownK130517 EZ Transport ChairHarris Medical, LLC · 2014
  9. Descendant · cites it directly · 0 of its ownK120405 Walk on Wheels HS-3500 Electric Aisle WheelchairWalk on Wheels Australia Pty, Ltd. · 2012

Most influential descendants

Showing 5 of 5 · See all
  • K111095Breeze Electric Transport Chair Model 1025Electro Kinetic Technologies, LLC · 2011 · cites it directly1descendant
  • K100327Heartway Power Chair, P23Heartway Medical Products Co., Ltd. · 2010 · cites it directly1descendant
  • K132856Heartway Power WheelchairHeartway Medical Products Co., Ltd. · 2014 · 2 generations on0descendants
  • K130517EZ Transport ChairHarris Medical, LLC · 2014 · 2 generations on0descendants
  • K120405Walk on Wheels HS-3500 Electric Aisle WheelchairWalk on Wheels Australia Pty, Ltd. · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K022697Teh Lin Jupiter Power Chair, Model TL-320Teh Lin Prosthetic & Orthopaedic, Inc.2003—
−2K061693Foryou Powered Wheelchair, Model FC-100Foryou Technology Co., Ltd.2006—
−1K070489Heartway Power Tilt Seating System Power Chair, Model# P16RTHeartway Medical Products Co., Ltd.2007—
0 (this device)K071006Heartway Attendant-Controlled Power Chair, TC1Heartway Medical Products Co., Ltd.2007—
+1K111095Breeze Electric Transport Chair Model 1025Electro Kinetic Technologies, LLC2011—
+1K100327Heartway Power Chair, P23Heartway Medical Products Co., Ltd.2010—
+2K132856Heartway Power WheelchairHeartway Medical Products Co., Ltd.2014—
+2K130517EZ Transport ChairHarris Medical, LLC2014—
+1K120405Walk on Wheels HS-3500 Electric Aisle WheelchairWalk on Wheels Australia Pty, Ltd.2012—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201110
201210
201420
FIG. 1 — Lineage of K071006, 2003–2014Source: 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 ITI? 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 ITI device

  1. #1 K220747 Power Wheelchair (N5515B)score 40.2 · 4 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
*K070489Heartway Power Tilt Seating System Power Chair, Model# P16RTHeartway Medical Products Co., Ltd.2007—

Also cleared against K070489: 2 other devices →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K111095Breeze Electric Transport Chair Model 1025Electro Kinetic Technologies, LLC20111
K100327Heartway Power Chair, P23Heartway Medical Products Co., Ltd.20101
K120405Walk on Wheels HS-3500 Electric Aisle WheelchairWalk on Wheels Australia Pty, Ltd.20120

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 4 years and passes through 3 companies; a new generation was cleared every 8 months on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K111095 (Electro Kinetic Technologies, LLC, 2011) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K070489.

How does its category compare?

All ITI devices

ITI Wheelchair, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · ITI

29in 2025

2007: 182008: 92009: 72010: 62011: 42012: 62013: 52014: 52015: 102016: 62017: 42018: 42019: 32020: 62021: 132022: 162023: 82024: 382025: 292026 (partial year): 36
2007high 38 (2024) · low 3 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ITI

90in 2025

2007: 42 days median2008: 49 days median2009: 63 days median2010: 46 days median2011: 101 days median2012: 155 days median2013: 177 days median2014: 213 days median2015: 174 days median2016: 173 days median2017: 159 days median2018: 117 days median2019: 244 days median2020: 278 days median2021: 209 days median2022: 96 days median2023: 128 days median2024: 125 days median2025: 90 days median2026 (partial year): 108 days median
2007high 278 (2020) · low 42 (2007)2026

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

Recalls per year · ITI

13so far in 2026, the most since 2007

2007: 32008: 32009: 12010: 22012: 12016: 12017: 22021: 32024: 12025: 3, 2 Class I2026 (partial year): 13
2007high 13 (2026) · low 0 (2011)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · ITI

647in 2025

2007: 1232008: 1332009: 1832010: 1572011: 5252012: 2,9192013: 8,7412014: 7,2822015: 4,6852016: 1,5752017: 3012018: 2732019: 2642020: 2052021: 1662022: 1352023: 2232024: 1462025: 647
2007high 8,741 (2013) · low 123 (2007)2025

MAUDE reports naming product code ITI, 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
200718423123
20089493133
20097631183
20106462157
201141010525
2012615512,919
2013517708,741
2014521307,282
20151017404,685
2016617311,575
201741592301
201841170273
201932440264
202062780205
2021132093166
202216960135
202381280223
2024381251146
202529903 (2)647
20263610813—

What is it indicated for?

The device is intended for medical purposes to provide mobility to persons restricted to

a sitting position.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071006: Heartway Attendant-Controlled Power Chair, TC1.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071006

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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