510(k) · Cleared
ClearedHoverjack Air Patient Lift Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
D.T. Davis Enterprises, Ltd. · FNG Lift, Patient, Ac-Powered
Cleared on Aug 12, 2004 as substantially equivalent to K926411 (Arjo-Century, Inc., 1993) after a 66-day review. Its family tree reaches back 1 generation to 1993. 1 later device descends from it.
- Decided
- Aug 12, 2004
- Review
- 66 days
- Class
- Class II
- Product code
- FNG
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K926411 (1993). 1 later device descends from it, 1 citing it directly.
Most influential descendants
Showing 1 of 1 · See all- K121287HT-WedgeD.T. Davis Enterprises Ltd. T/A Hovertech Int'L · 2012 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K926411 | Saf-Lift/Saf-Kary | Arjo-Century, Inc. | 1993 | — |
| 0 (this device) | K041503 | Hoverjack Air Patient Lift Device | D.T. Davis Enterprises, Ltd. | 2004 | — |
| +1 | K121287 | HT-Wedge | D.T. Davis Enterprises Ltd. T/A Hovertech Int'L | 2012 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 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 FNG? 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
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K926411 | Saf-Lift/Saf-KarySummary page 1…hovermatt(a),eartlhink.net Predicate Device: Arjo-Century, Inc. Saf-Lift/Saf-Kary 510(k) #926411 1993 Intended Use: The HoverJackTM lifts a patient in a supine position, from the floor to the approximate height of a bed… | 1993 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K121287 | HT-Wedge | 2012 | 0 |
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.
- Of its descendants, K121287 (D.T. Davis Enterprises Ltd. T/A Hovertech Int'L, 2012) has gone furthest, with 0 descendants of its own.
How does its category compare?
All FNG devicesFNG Lift, Patient, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FNG
1in 2012
2026 to Oct 25, outlined.
Median 510(k) review, days · FNG
Too few FNG 510(k)s in any year since 2007 to give a median.
Recalls per year · FNG
1in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FNG
5in 2025
MAUDE reports naming product code FNG, 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 | 0 | — | 0 | 74 |
| 2008 | 0 | — | 1 | 125 |
| 2009 | 0 | — | 14 | 178 |
| 2010 | 0 | — | 0 | 95 |
| 2011 | 0 | — | 1 | 125 |
| 2012 | 1 | — | 0 | 93 |
| 2013 | 0 | — | 0 | 157 |
| 2014 | 0 | — | 0 | 51 |
| 2015 | 0 | — | 0 | 31 |
| 2016 | 0 | — | 0 | 5 |
| 2017 | 0 | — | 0 | 8 |
| 2018 | 0 | — | 0 | 6 |
| 2019 | 0 | — | 0 | 4 |
| 2020 | 0 | — | 0 | 5 |
| 2021 | 0 | — | 0 | 4 |
| 2022 | 0 | — | 1 | 5 |
| 2023 | 0 | — | 0 | 16 |
| 2024 | 0 | — | 0 | 4 |
| 2025 | 0 | — | 0 | 5 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The HoverJack TM lifts a patient in a supine position, from the floor to the approximate height of a bed for a subsequent lateral patient transfer.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K041503 · printed Nov 6, 2026
Cite this page
510(k) Report. “K041503: Hoverjack Air Patient Lift Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K041503
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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