510(k) · Cleared
ClearedIrsg I-Mover for Beds
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
International Retail Services Group, LLC · FPO Stretcher, Wheeled
Cleared on Apr 14, 2008 as substantially equivalent to K022309 (Stryker Corp., 2002) after a 213-day review. Its family tree reaches back 2 generations to 1995. 1 later device descends from it.
- Decided
- Apr 14, 2008
- Review
- 213 days
- Class
- Class II
- Product code
- FPO
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K942948 (1995). 1 later device descends from it, 1 citing it directly.
- Root · 2 generations backK942948 Stryker Powered StretcherStryker Corp. · 1995
- 1 generation backK022309 Stryker Powered Wheeled StretcherStryker Corp. · 2002 · Recalled
- This deviceK072598 Irsg I-Mover for BedsInternational Retail Services Group, LLC · 2008
- Descendant · cites it directly · 0 of its ownK113598 Power-Load Cot Fastener SystemStryker Medical · 2011 · Recalled
Most influential descendants
Showing 1 of 1 · See all- K113598Power-Load Cot Fastener SystemStryker Medical · 2011 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K942948 | Stryker Powered Stretcher | Stryker Corp. | 1995 | — |
| −1 | K022309 | Stryker Powered Wheeled Stretcher | Stryker Corp. | 2002 | 6 |
| 0 (this device) | K072598 | Irsg I-Mover for Beds | International Retail Services Group, LLC | 2008 | — |
| +1 | K113598 | Power-Load Cot Fastener System | Stryker Medical | 2011 | 3 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 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 FPO? 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? (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 |
|---|---|---|---|
| * | K022309 | Stryker Powered Wheeled StretcherSummary page 1…The IRSG bed mover is substantially equivalent to the Stryker ZoomTM Motorized Stretchers ,(i.e. with the Stryker Powered Wheeled Stretcher with a drive option)K022309 and the Paramed Systems ParaglydeTM DCS - TM1 (FPO, 880.6910, Class II, 510k exempt) in function, technological characteristi… | 2002 |
| * | — | Paramed Systems Paraglyde™ DCS™-1 Named without a submission number |
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 |
|---|---|---|---|
| K113598 | Power-Load Cot Fastener System | 2011 | 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?
- The line of descent spans 13 years and passes through 2 companies; a new generation was cleared every 7.8 years on median.
- 1 of the 2 ancestors has a recall of any class.
- Of its descendants, K113598 (Stryker Medical, 2011) has gone furthest, with 0 descendants of its own.
- 5 other devices also cite its predicate K022309.
How does its category compare?
All FPO devicesFPO Stretcher, Wheeled: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.
FDA decisions per year · FPO
1in 2011
2026 to Oct 25, outlined.
Median 510(k) review, days · FPO
Too few FPO 510(k)s in any year since 2007 to give a median.
Recalls per year · FPO
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FPO
897in 2025
MAUDE reports naming product code FPO, 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 | — | 6 | 117 |
| 2008 | 1 | — | 3 | 385 |
| 2009 | 0 | — | 12 | 2,337 |
| 2010 | 0 | — | 1 | 4,049 |
| 2011 | 1 | — | 6 | 5,891 |
| 2012 | 0 | — | 1 | 6,334 |
| 2013 | 0 | — | 0 | 5,743 |
| 2014 | 0 | — | 1 | 1,633 |
| 2015 | 0 | — | 0 | 381 |
| 2016 | 0 | — | 1 | 205 |
| 2017 | 0 | — | 0 | 230 |
| 2018 | 0 | — | 0 | 573 |
| 2019 | 0 | — | 0 | 663 |
| 2020 | 0 | — | 0 | 694 |
| 2021 | 0 | — | 0 | 874 |
| 2022 | 0 | — | 2 | 694 |
| 2023 | 0 | — | 0 | 1,028 |
| 2024 | 0 | — | 0 | 956 |
| 2025 | 0 | — | 1 | 897 |
| 2026 | 0 | — | 2 | — |
What is it indicated for?
The bed mover is intended to assist a single operator in the moving of wheeled beds and stretchers from one location to another within a healthcare facility.
Examples of usage include:
- a single operator may move empty beds to staging or storage areas within the healthcare facility.
- a single operator may move patient-laden beds from one location to another within the healthcare facility.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K072598 · printed Nov 4, 2026
Cite this page
510(k) Report. “K072598: Irsg I-Mover for Beds.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K072598
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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