510(k) · Cleared
ClearedRecovery Pump 737R
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Mego Afek AC, Ltd. · IRP Massager, Powered Inflatable Tube
Cleared on Jun 16, 2014 after a 108-day review. The FDA summary names no predicate by number. 5 later devices descend from it.
- Decided
- Jun 16, 2014
- Review
- 108 days
- Class
- Class II
- Product code
- IRP
- Recalls
- None
- Predicates
- 0
5 later devices descend from it, 1 citing it directly.
- This deviceK140519 Recovery Pump 737RMego Afek AC, Ltd. · 2014
- Descendant · cites it directly · 4 of its ownK211745 RecoveryAir PROTheragun, Inc. · 2021
- Descendant · 2 generations on · 1 of its ownK241256 JetBoots PRO PlusTherabody, Inc. · 2024
- Descendant · 3 generations on · 0 of its ownK242140 Air Compression Leg Massager (K-705)Jiale Health Technology Shenzhen Co., Ltd. · 2025
- Descendant · 2 generations on · 0 of its ownK243206 Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3…Sichuan Qianli-Beoka Medical Technology, Inc. · 2025
- Descendant · 2 generations on · 0 of its ownK233238 Air Pressure Therapy System (Model:VU-IPC4M)Xiamen Weiyou Intelligent Technology Co., Ltd. · 2024
Most influential descendants
Showing 5 of 5 · See all- K211745RecoveryAir PROTheragun, Inc. · 2021 · cites it directly4descendants
- K241256JetBoots PRO PlusTherabody, Inc. · 2024 · 2 generations on1descendant
- K242140Air Compression Leg Massager (K-705)Jiale Health Technology Shenzhen Co., Ltd. · 2025 · 3 generations on0descendants
- K243206Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4…Sichuan Qianli-Beoka Medical Technology, Inc. · 2025 · 2 generations on0descendants
- K233238Air Pressure Therapy System (Model:VU-IPC4M)Xiamen Weiyou Intelligent Technology Co., Ltd. · 2024 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K140519 | Recovery Pump 737R | Mego Afek AC, Ltd. | 2014 | — |
| +1 | K211745 | RecoveryAir PRO | Theragun, Inc. | 2021 | — |
| +2 | K241256 | JetBoots PRO Plus | Therabody, Inc. | 2024 | — |
| +3 | K242140 | Air Compression Leg Massager (K-705) | Jiale Health Technology Shenzhen Co., Ltd. | 2025 | — |
| +2 | K243206 | Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4… | Sichuan Qianli-Beoka Medical Technology, Inc. | 2025 | — |
| +2 | K233238 | Air Pressure Therapy System (Model:VU-IPC4M) | Xiamen Weiyou Intelligent Technology Co., Ltd. | 2024 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2021 | 1 | 0 |
| 2024 | 2 | 0 |
| 2025 | 2 | 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 IRP? 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 IRP device
- #1 K193354 Air Compression Therapy Devicescore 28.6 · 8 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
The FDA summary names no predicate by number.
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K211745 | RecoveryAir PRO | 2021 | 4 |
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, K211745 (Theragun, Inc., 2021) has gone furthest, with 4 descendants of its own.
How does its category compare?
All IRP devicesIRP Massager, Powered Inflatable Tube: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · IRP
13in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IRP
141in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IRP
2in 2017
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IRP
10in 2025
MAUDE reports naming product code IRP, 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 | 2 | — | 0 | 0 |
| 2008 | 1 | — | 0 | 2 |
| 2009 | 1 | — | 0 | 1 |
| 2010 | 2 | — | 0 | 5 |
| 2011 | 3 | 164 | 1 | 3 |
| 2012 | 5 | 116 | 0 | 3 |
| 2013 | 2 | — | 0 | 0 |
| 2014 | 4 | 113 | 0 | 0 |
| 2015 | 2 | — | 0 | 3 |
| 2016 | 1 | — | 0 | 2 |
| 2017 | 4 | 170 | 2 | 0 |
| 2018 | 3 | 80 | 0 | 0 |
| 2019 | 10 | 83 | 0 | 0 |
| 2020 | 9 | 150 | 0 | 1 |
| 2021 | 19 | 140 | 0 | 0 |
| 2022 | 14 | 97 | 0 | 1 |
| 2023 | 10 | 143 | 0 | 0 |
| 2024 | 12 | 115 | 0 | 4 |
| 2025 | 13 | 141 | 0 | 10 |
| 2026 | 12 | 172 | 0 | — |
What is it indicated for?
The Recovery Pump 737R1 is an air compression therapy device intended to provide graduated pressure to compression garments.
The Recovery Pump 737R is indicated for the temporary relief of minor muscle aches and pains, and for temporary increase in blood circulation to the treated areas in people who are in good health, The Recovery Pump 737R simulates kneading and stroking of tissues by using an inflatable garment.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K140519 · printed Nov 6, 2026
Cite this page
510(k) Report. “K140519: Recovery Pump 737R.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140519
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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