510(k) · Cleared
ClearedVaso Press DVT Foot Garment #VP 520
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Britt Corp., Inc. · JOW Sleeve, Limb, Compressible
Cleared on May 18, 2001 after a 158-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 5 later devices descend from it.
- Decided
- May 18, 2001
- Review
- 158 days
- Class
- Class II
- Product code
- JOW
- Recalls
- None
- Predicates
- 0
5 later devices descend from it, 3 citing it directly.
- This deviceK003828 Vaso Press DVT Foot Garment #VP 520Britt Corp., Inc. · 2001
- Descendant · cites it directly · 3 of its ownK112838 Vasopress Reprocessed DVT Leg / Foot GarmentsCompression Therapy Concepts, Inc. · 2011
- Descendant · 2 generations on · 1 of its ownK201547 B&J DVT Foot Garments, Models 820 SeriesB&J Manufacturing, Ltd. · 2020
- Descendant · 3 generations on · 0 of its ownK253386 DVT GarmentVistar Medical Supplies Co., Ltd. · 2026
- Descendant · cites it directly · 0 of its ownK122179 Vasopress DVT Leg Garments (Sterile) Vasopress DVT Foot Garments…Compression Therapy Concepts · 2012
- Descendant · cites it directly · 0 of its ownK052691 Suretek Medical Reprocessed Compression SleevesSuretek Medical · 2006
Most influential descendants
Showing 5 of 5 · See all- K112838Vasopress Reprocessed DVT Leg / Foot GarmentsCompression Therapy Concepts, Inc. · 2011 · cites it directly3descendants
- K201547B&J DVT Foot Garments, Models 820 SeriesB&J Manufacturing, Ltd. · 2020 · 2 generations on1descendant
- K253386DVT GarmentVistar Medical Supplies Co., Ltd. · 2026 · 3 generations on0descendants
- K122179Vasopress DVT Leg Garments (Sterile) Vasopress DVT Foot Garments (Sterile)Compression Therapy Concepts · 2012 · cites it directly0descendants
- K052691Suretek Medical Reprocessed Compression SleevesSuretek Medical · 2006 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K003828 | Vaso Press DVT Foot Garment #VP 520 | Britt Corp., Inc. | 2001 | — |
| +1 | K112838 | Vasopress Reprocessed DVT Leg / Foot Garments | Compression Therapy Concepts, Inc. | 2011 | — |
| +2 | K201547 | B&J DVT Foot Garments, Models 820 Series | B&J Manufacturing, Ltd. | 2020 | — |
| +3 | K253386 | DVT Garment | Vistar Medical Supplies Co., Ltd. | 2026 | — |
| +1 | K122179 | Vasopress DVT Leg Garments (Sterile) Vasopress DVT Foot Garments (Sterile) | Compression Therapy Concepts | 2012 | — |
| +1 | K052691 | Suretek Medical Reprocessed Compression Sleeves | Suretek Medical | 2006 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2011 | 1 | 0 |
| 2012 | 1 | 0 |
| 2020 | 1 | 0 |
| 2026 | 1 | 0 |
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 JOW? 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 JOW device
- #1 K253555 Flexitouch® Plus Advanced Pneumatic…score 14.8 · 11 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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? (5)
3 later devices cite it directly; ranked here by how many devices descend from each in turn.
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, K112838 (Compression Therapy Concepts, Inc., 2011) has gone furthest, with 3 descendants of its own.
How does its category compare?
All JOW devicesJOW Sleeve, Limb, Compressible: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JOW
7in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JOW
168in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JOW
1in 2019
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JOW
24in 2025
MAUDE reports naming product code JOW, 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 | 6 | 66 | 0 | 12 |
| 2008 | 4 | 112 | 7 | 36 |
| 2009 | 3 | 84 | 0 | 45 |
| 2010 | 18 | 71 | 2 | 66 |
| 2011 | 11 | 104 | 3 | 50 |
| 2012 | 13 | 63 | 2 | 100 |
| 2013 | 17 | 94 | 0 | 169 |
| 2014 | 16 | 91 | 0 | 93 |
| 2015 | 10 | 160 | 0 | 137 |
| 2016 | 9 | 121 | 0 | 150 |
| 2017 | 9 | 116 | 1 | 149 |
| 2018 | 11 | 136 | 0 | 114 |
| 2019 | 11 | 88 | 1 | 102 |
| 2020 | 14 | 158 | 0 | 50 |
| 2021 | 16 | 132 | 0 | 34 |
| 2022 | 7 | 80 | 0 | 27 |
| 2023 | 6 | 160 | 0 | 57 |
| 2024 | 8 | 197 | 0 | 30 |
| 2025 | 7 | 168 | 0 | 24 |
| 2026 | 6 | 252 | 0 | — |
https://510kreport.com/device/K003828 · printed Nov 6, 2026
Cite this page
510(k) Report. “K003828: Vaso Press DVT Foot Garment #VP 520.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K003828
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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