510(k) · Cleared
ClearedANGIO-PRESS DVT Compression Device Model Name: IPCS
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Pegasus Medical Supply, Inc. · JOW Sleeve, Limb, Compressible
Cleared on Jul 7, 2015 as substantially equivalent to K101915 (Compression Therapy Concepts, Inc., 2010) after a 242-day review. Its family tree reaches back 1 generation to 2010. 1 later device descends from it.
- Decided
- Jul 7, 2015
- Review
- 242 days
- Class
- Class II
- Product code
- JOW
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K101915 (2010). 1 later device descends from it, 1 citing it directly.
- Root · 1 generation backK101915 Vasopress Supreme Mini Model VP500DMCompression Therapy Concepts, Inc. · 2010
- This deviceK143202 ANGIO-PRESS DVT Compression Device Model Name: IPCSPegasus Medical Supply, Inc. · 2015
- Descendant · cites it directly · 0 of its ownK173012 ANGIO-PRESS LITE DVT Compression DevicePegasus Medical Supply, Inc. · 2018
Most influential descendants
Showing 1 of 1 · See all- K173012ANGIO-PRESS LITE DVT Compression DevicePegasus Medical Supply, Inc. · 2018 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K101915 | Vasopress Supreme Mini Model VP500DM | Compression Therapy Concepts, Inc. | 2010 | — |
| 0 (this device) | K143202 | ANGIO-PRESS DVT Compression Device Model Name: IPCS | Pegasus Medical Supply, Inc. | 2015 | — |
| +1 | K173012 | ANGIO-PRESS LITE DVT Compression Device | Pegasus Medical Supply, Inc. | 2018 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 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 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? (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 |
|---|---|---|---|
| * | K101915 | Vasopress Supreme Mini Model VP500DMSummary page 4…Compression Therapy Concepts, Inc. Regulation number: 870.5800 Product Code: JOW 510(k) Number: K101915 лй Pegasus Medical… | 2010 |
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 |
|---|---|---|---|
| K173012 | ANGIO-PRESS LITE DVT Compression Device | 2018 | 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, K173012 (Pegasus Medical Supply, Inc., 2018) has gone furthest, with 0 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. 2015, this device’s year, is highlighted.
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 | — |
What is it indicated for?
The Pegasus Medical Supply Inc. ANGIO-PRESS IPCS Deep Vein Thrombosis (DVT) Compression Devices are intended to increase venous blood flow in patients in order to help prevent deep vein thrombosis.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K143202 · printed Nov 6, 2026
Cite this page
510(k) Report. “K143202: ANGIO-PRESS DVT Compression Device Model Name: IPCS.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K143202
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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