510(k) Report

510(k) · Cleared

Cleared

Action at Manual Wheelchair

K941989510(k) TraditionalCleared May 11, 199416-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

Nvacare Corp. · IOR Wheelchair, Mechanical

Cleared on May 11, 1994 after a 16-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 14 later devices descend from it.

Decided
May 11, 1994
Review
16 days
Class
Class I
Product code
IOR
Recalls
None
Predicates
0

14 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1999: 1 descendant cleared2001: 1 descendant cleared2018: 1 descendant cleared2007: 1 descendant cleared2010: 2 descendants cleared2008: 2 descendants cleared2004: 1 descendant cleared2013: 2 descendants cleared2012: 1 descendant cleared2016: 1 descendant cleared2023: 1 descendant cleared1990200020102020
  1. This deviceK941989 Action at Manual WheelchairNvacare Corp. · 1994
  2. Descendant · cites it directly · 13 of its ownK984447 Model Action at II Manual WheelchairInvacare Corp. · 1999 · Recalled
  3. Descendant · 2 generations on · 6 of its ownK012370 Solara JR. Manual WheelchairInvacare Corp. · 2001 · Recalled
  4. Descendant · 2 generations on · 4 of its ownK063736 Fuze Mechanical Wheelchair, Models T20 and T50Pdg Product Design Group, Inc. · 2007 · Recalled
  5. Descendant · 3 generations on · 2 of its ownK043332 Wheelchair, Model 8500-IICycling and Health Tech. Industry R&D Center · 2004
  6. Descendant · 2 generations on · 1 of its ownK181090 Invacare® Solara® 3G and Solara® 3G Spree Manual WheelchairsInvacare Corporation · 2018

Showing 5 of 14 descendants. See all descendants

Descendants cleared per year

1999: 12001: 12004: 12007: 12008: 22010: 22012: 12013: 22016: 12018: 12023: 1
1999high 2 (2008) · low 0 (2000)2026

Most influential descendants

Showing 5 of 14 · See all
  • K984447Model Action at II Manual WheelchairInvacare Corp. · 1999 · cites it directly13descendants
  • K012370Solara JR. Manual WheelchairInvacare Corp. · 2001 · 2 generations on6descendants
  • K063736Fuze Mechanical Wheelchair, Models T20 and T50Pdg Product Design Group, Inc. · 2007 · 2 generations on4descendants
  • K043332Wheelchair, Model 8500-IICycling and Health Tech. Industry R&D Center · 2004 · 3 generations on2descendants
  • K181090Invacare® Solara® 3G and Solara® 3G Spree Manual WheelchairsInvacare Corporation · 2018 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K941989Action at Manual WheelchairNvacare Corp.1994—
+1K984447Model Action at II Manual WheelchairInvacare Corp.19991
+2K012370Solara JR. Manual WheelchairInvacare Corp.20013
+2K063736Fuze Mechanical Wheelchair, Models T20 and T50Pdg Product Design Group, Inc.20071
+3K043332Wheelchair, Model 8500-IICycling and Health Tech. Industry R&D Center2004—
+2K181090Invacare® Solara® 3G and Solara® 3G Spree Manual WheelchairsInvacare Corporation2018—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
200110
200410
200710
200820
201020
201210
201320
201610
201810
202310
FIG. 1 — Lineage of K941989, 1994–2023Source: 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), 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (14)

See all 14

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K984447Model Action at II Manual WheelchairInvacare Corp.199913

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?

  • Of its descendants, K984447 (Invacare Corp., 1999) has gone furthest, with 13 descendants of its own.

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—
Cite this page

510(k) Report. “K941989: Action at Manual Wheelchair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K941989

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026