510(k) · Cleared
ClearedCombat Ready Clamp
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Combat Medical Systems, LLC · DXC Clamp, Vascular
Cleared on Apr 29, 2013 as substantially equivalent to K102025 (Combat Medical Systems, LLC, 2010) after a 63-day review. Its family tree reaches back 2 generations to 2000. 4 later devices descend from it.
- Decided
- Apr 29, 2013
- Review
- 63 days
- Class
- Class II
- Product code
- DXC
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K002767 (2000). 4 later devices descend from it, 2 citing it directly.
- Root · 2 generations backK002767 Compressar Femoral Access Compression DeviceSemler Technologies, Inc. · 2000
- 1 generation backK102025 Combat Ready ClampCombat Medical Systems, LLC · 2010
- This deviceK130482 Combat Ready ClampCombat Medical Systems, LLC · 2013
- Descendant · cites it directly · 1 of its ownK141685 CROCCombat Medical Systems, LLC · 2015
- Descendant · cites it directly · 1 of its ownK133029 Abdominal Aortic and Junctional Tourniquet (Aajt) DeviceCompression Works, LLC · 2013
- Descendant · 2 generations on · 0 of its ownK243627 Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial…Arc Trauma, LLC · 2025
- Descendant · 2 generations on · 0 of its ownK221661 Abdominal Aortic and Junctional Tourniquet - Stabilized (AAJT-S)Compression Works, Inc. · 2023
Most influential descendants
Showing 4 of 4 · See all- K141685CROCCombat Medical Systems, LLC · 2015 · cites it directly1descendant
- K133029Abdominal Aortic and Junctional Tourniquet (Aajt) DeviceCompression Works, LLC · 2013 · cites it directly1descendant
- K243627Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp…Arc Trauma, LLC · 2025 · 2 generations on0descendants
- K221661Abdominal Aortic and Junctional Tourniquet - Stabilized (AAJT-S)Compression Works, Inc. · 2023 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K002767 | Compressar Femoral Access Compression Device | Semler Technologies, Inc. | 2000 | — |
| −1 | K102025 | Combat Ready Clamp | Combat Medical Systems, LLC | 2010 | — |
| 0 (this device) | K130482 | Combat Ready Clamp | Combat Medical Systems, LLC | 2013 | — |
| +1 | K141685 | CROC | Combat Medical Systems, LLC | 2015 | — |
| +1 | K133029 | Abdominal Aortic and Junctional Tourniquet (Aajt) Device | Compression Works, LLC | 2013 | — |
| +2 | K243627 | Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial… | Arc Trauma, LLC | 2025 | — |
| +2 | K221661 | Abdominal Aortic and Junctional Tourniquet - Stabilized (AAJT-S) | Compression Works, Inc. | 2023 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
| 2015 | 1 | 0 |
| 2023 | 1 | 0 |
| 2025 | 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 DXC? 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 DXC device
- #1 K262086 PreludeSYNC™ Radial Compression Devicescore 13.5 · 7 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 |
|---|---|---|---|
| * | K102025 | Combat Ready ClampSummary page 1…21 CFR 870.4450, Class 11, 510(k) Panel: Cardiovascular Product Code: DXC Predicate Device: K 102025, Combat Ready Clamp Indication for Use: The Combat Ready Clamp (CRoCTM) is indicated for use in the battlefield to control diffi… | 2010 |
What descends from it? (4)
2 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?
- The line of descent spans 13 years and passes through 2 companies; a new generation was cleared every 9.9 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K141685 (Combat Medical Systems, LLC, 2015) has gone furthest, with 1 descendant of its own.
- 4 other devices also cite its predicate K102025.
How does its category compare?
All DXC devicesDXC Clamp, Vascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · DXC
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DXC
215in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DXC
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DXC
442in 2025
MAUDE reports naming product code DXC, 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 | 10 | 52 | 0 | 298 |
| 2008 | 3 | 29 | 2 | 302 |
| 2009 | 4 | 83 | 2 | 539 |
| 2010 | 2 | — | 1 | 600 |
| 2011 | 6 | 51 | 3 | 691 |
| 2012 | 5 | 73 | 0 | 548 |
| 2013 | 14 | 89 | 0 | 920 |
| 2014 | 4 | 157 | 1 | 494 |
| 2015 | 5 | 71 | 0 | 374 |
| 2016 | 3 | 91 | 0 | 494 |
| 2017 | 3 | 90 | 0 | 416 |
| 2018 | 2 | — | 0 | 391 |
| 2019 | 2 | — | 0 | 393 |
| 2020 | 3 | 209 | 0 | 404 |
| 2021 | 6 | 37 | 0 | 371 |
| 2022 | 1 | — | 1 | 273 |
| 2023 | 4 | 215 | 2 | 674 |
| 2024 | 1 | — | 0 | 375 |
| 2025 | 2 | — | 0 | 442 |
| 2026 | 4 | 125 | 0 | — |
What is it indicated for?
The Combat Ready Clamp is indicated for use in the battlefield to control difficult bleeds in the inguinal and axilla areas.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K130482 · printed Nov 6, 2026
Cite this page
510(k) Report. “K130482: Combat Ready Clamp.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K130482
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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