510(k) · Cleared
ClearedPlexus SCD110 Sequential Compression Device Sleeve
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Midway Medical, LLC · JOW Sleeve, Limb, Compressible
Cleared on Jul 22, 2019 as substantially equivalent to K141578 (Devon Medical, 2014) after a 98-day review. Its family tree reaches back 4 generations to 2000.
- Decided
- Jul 22, 2019
- Review
- 98 days
- Class
- Class II
- Product code
- JOW
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K991038 (2000). 6 ancestors in all, the oldest K961166 (1996). No later device cites it as a predicate yet.
- Root · 4 generations backK991038 Vaso Press DVT System, Models VP500, VP501Britt Corp., Inc. · 2000
- 3 generations backK090308 Restep Dvy System, Model RSP-101Stortford Medical, LLC · 2009 · Recalled
- 2 generations backK130571 Devon Cirona 6100 DVTDevon Medical, Inc. · 2013
- 1 generation backK141578 Devon Cirona 6200 DVTDevon Medical · 2014
- This deviceK190975 Plexus SCD110 Sequential Compression Device SleeveMidway Medical, LLC · 2019
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K991038 | Vaso Press DVT System, Models VP500, VP501 | Britt Corp., Inc. | 2000 | — |
| −3 | K090308 | Restep Dvy System, Model RSP-101 | Stortford Medical, LLC | 2009 | 1 |
| −2 | K130571 | Devon Cirona 6100 DVT | Devon Medical, Inc. | 2013 | — |
| −1 | K141578 | Devon Cirona 6200 DVT | Devon Medical | 2014 | — |
| 0 (this device) | K190975 | Plexus SCD110 Sequential Compression Device Sleeve | Midway Medical, LLC | 2019 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 2002 | 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 |
|---|---|---|---|
| * | K141578 | Devon Cirona 6200 DVTSummary page 4…Product Manufacturer 510(k) Number Cirona 6200 DVT Sleeves Devon Medical Products K141578 Reference Devices: Product Manufacturer 510(k) Number Excel… | 2014 |
| † | K133119 | Flowtron ACS800 Pump and Tri Pulse Garments | 2014 |
| † | K122499 | Aircast Venaflow Elite System | 2012 |
| † | K110358 | Venodyne V810 | 2011 |
| † | K101915 | Vasopress Supreme Mini Model VP500DM | 2010 |
What descends from it?
No later submission names this one as a predicate yet.
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 19 years and passes through 5 companies; a new generation was cleared every 5.1 years on median.
- 2 of the 6 ancestors have a recall of any class.
- 3 other devices also cite its predicate K141578.
How does its category compare?
All JOW devicesJOW Sleeve, Limb, Compressible: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, 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 Plexus SCD 110 DVT Sleeve is a prescription device intended to be used preventatively to increase venous blood flow in patients at risk of deep vein thrombosis due to the associated risk factors for thrombus formation during: trauma, critical care, general medicine, general surgery, as well as neurological, orthopedic, urologic, obstetric conditions and treatments.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K190975 · printed Nov 4, 2026
Cite this page
510(k) Report. “K190975: Plexus SCD110 Sequential Compression Device Sleeve.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K190975
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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