510(k) · Cleared
ClearedF5 Corpus VS
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Permobil AB · IPL Wheelchair, Standup
Cleared on Oct 25, 2019 as substantially equivalent to K172384 (Sunrise Medical (Us), LLC, 2018) and 1 other predicate after a 105-day review. Its family tree reaches back 6 generations to 1997.
- Decided
- Oct 25, 2019
- Review
- 105 days
- Class
- Class II
- Product code
- IPL
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 6 generations to K960951 (1997). 13 ancestors in all. No later device cites it as a predicate yet.
- Root · 6 generations backK960951 Permobil Chairman L/CS 8Permobil AB · 1997
- 5 generations backK991658 Permobil Powered Wheelchair 1280Permobil AB · 1999 · Recalled
- 4 generations backK041219 ElectroPermobil AB · 2004 · Recalled
- 3 generations backK071650 C350 Powered WheelchairPermobil AB · 2007 · Recalled
- 2 generations backK103477 Permobil M300 / M400Permobil AB · 2011
- 1 generation backK143014 F5Permobil AB · 2015
- This deviceK191874 F5 Corpus VSPermobil AB · 2019
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K960951 | Permobil Chairman L/CS 8 | Permobil AB | 1997 | — |
| −5 | K991658 | Permobil Powered Wheelchair 1280 | Permobil AB | 1999 | 5 |
| −4 | K041219 | Electro | Permobil AB | 2004 | 4 |
| −3 | K071650 | C350 Powered Wheelchair | Permobil AB | 2007 | 3 |
| −2 | K103477 | Permobil M300 / M400 | Permobil AB | 2011 | — |
| −1 | K143014 | F5 | Permobil AB | 2015 | — |
| 0 (this device) | K191874 | F5 Corpus VS | Permobil AB | 2019 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 2003 | 2 | 0 |
| 2005 | 1 | 0 |
| 2008 | 1 | 0 |
| 2018 | 1 | 0 |
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 IPL? 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 IPL device
- #1 K203761 ParaMotionscore 3.3 · 3 generations · no Class I recall
- #2 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K172384 | Quickie (r) Q700-UP MSummary page 4…andup Classification Name: Standup Wheelchair Primary Product Code (Standup feature): IPL Secondary Product Code: ITI Predicate Device: Primary: Quickie® Q700-UP M (K172384) manufactured by Sunrise Medical (US) LLC Secondary: F5 (K143014) manufactured by Permobil AB. Description of the F5 Corpus VS:… | 2018 |
| * | K143014 | F5Summary page 4…ode (Standup feature): IPL Secondary Product Code: ITI Predicate Device: Primary: Quickie® Q700-UP M (K172384) manufactured by Sunrise Medical (US) LLC Secondary: F5 (K143014) manufactured by Permobil AB. Description of the F5 Corpus VS: This submission covers the F5 Corpus VS device. Indications for… | 2015 |
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?
- The line of descent spans 22 years and passes through 1 company; a new generation was cleared every 4.1 years on median.
- 4 of the 13 ancestors have a recall of any class.
- 1 other device also cites its predicate K172384.
How does its category compare?
All IPL devicesIPL Wheelchair, Standup: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · IPL
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IPL
105in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IPL
No recall names IPL since 2007.
Adverse event reports per year · IPL
5in 2025
MAUDE reports naming product code IPL, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 3 | 63 | 0 | 0 |
| 2008 | 1 | — | 0 | 1 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 2 | — | 0 | 1 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 3 |
| 2014 | 0 | — | 0 | 1 |
| 2015 | 1 | — | 0 | 3 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 2 | — | 0 | 1 |
| 2019 | 3 | 105 | 0 | 1 |
| 2020 | 2 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 4 |
| 2022 | 2 | — | 0 | 3 |
| 2023 | 0 | — | 0 | 9 |
| 2024 | 0 | — | 0 | 6 |
| 2025 | 1 | — | 0 | 5 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The F5 Corpus VS powered wheelchair is to provide indoor and outdoor mobility, including stand-up feature, to persons limited to a seating position that are capable of operating a powered wheelchair.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K191874 · printed Nov 5, 2026
Cite this page
510(k) Report. “K191874: F5 Corpus VS.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K191874
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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