510(k) · Cleared
ClearedArtimes Balloon Dilatation Catheter
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Brosmed Medical · LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
Cleared on Sep 12, 2014 as substantially equivalent to P790017 (Medtronic, Ireland, 1980) and 3 other predicates after a 144-day review. Its family tree reaches back 1 generation to 1980. 1 later device descends from it.
- Decided
- Sep 12, 2014
- Review
- 144 days
- Class
- Class II
- Product code
- LOX
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 1 generation to P790017 (1980). 4 ancestors in all. 1 later device descends from it, 1 citing it directly.
Most influential descendants
Showing 1 of 1 · See all- K203390Artimes pro Balloon Dilatation CatheterBrosmed Medical Co., Ltd. · 2021 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | P790017 | Usci Dilatation Catheter | Medtronic, Ireland | 1980 | — |
| 0 (this device) | K141025 | Artimes Balloon Dilatation Catheter | Brosmed Medical | 2014 | — |
| +1 | K203390 | Artimes pro Balloon Dilatation Catheter | Brosmed Medical Co., Ltd. | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1982 | 1 | 0 |
| 1986 | 1 | 0 |
| 1988 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2021 | 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 LOX? 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 LOX device
- #1 K254022 FLASH Flex™ Aorto-Ostial Angioplasty Systemscore 12.3 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (4)
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 |
|---|---|---|---|
| * | P790017 | Usci Dilatation CatheterSummary page 4…al coronary angioplasty, percutaneous (21 CFR 870.5100(a), Product Code LOX) Predicate Devices: Sprinter Legend RX (P790017 S096; cleared October 31, 2008) Voyager RX (P810046 S216; cleared June 18, 2004)… | 1980 |
| * | P810046 | Simpson-Robert Coronary Balloon Dilatation CatheteSummary page 4…00(a), Product Code LOX) Predicate Devices: Sprinter Legend RX (P790017 S096; cleared October 31, 2008) Voyager RX (P810046 S216; cleared June 18, 2004) Maverick (P860019 S160; cleared September 27, 2000)… | 1982 |
| * | P860019 | Scimed Ptca Dilatation CatheterSummary page 4…790017 S096; cleared October 31, 2008) Voyager RX (P810046 S216; cleared June 18, 2004) Maverick (P860019 S160; cleared September 27, 2000) Apex (P860019 S208; cleared November 7, 2008)… | 1986 |
| * | P880003 | Cordis Ptca Dilatation CatheterSummary page 4…860019 S160; cleared September 27, 2000) Apex (P860019 S208; cleared November 7, 2008) Fire Star (P880003 S090; cleared August 31, 2007) Device Description: The Artimes1 (Rx type) device is a coronary dilatation cathet… | 1988 |
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 |
|---|---|---|---|
| K203390 | Artimes pro Balloon Dilatation Catheter | 2021 | 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?
How does its category compare?
All LOX devicesLOX Catheters, Transluminal Coronary Angioplasty, Percutaneous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · LOX
4in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · LOX
241in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LOX
4in 2019
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LOX
1,890in 2025
MAUDE reports naming product code LOX, 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 | 19 | — | 1 | 1,053 |
| 2008 | 22 | — | 80 | 1,063 |
| 2009 | 28 | — | 0 | 1,353 |
| 2010 | 32 | — | 0 | 1,392 |
| 2011 | 9 | 103 | 0 | 2,090 |
| 2012 | 10 | 120 | 0 | 2,092 |
| 2013 | 6 | 123 | 0 | 2,436 |
| 2014 | 6 | 166 | 0 | 2,316 |
| 2015 | 4 | 119 | 0 | 2,060 |
| 2016 | 9 | 116 | 0 | 2,578 |
| 2017 | 6 | 113 | 0 | 2,753 |
| 2018 | 7 | 80 | 0 | 2,225 |
| 2019 | 1 | — | 4 | 2,102 |
| 2020 | 1 | — | 0 | 1,974 |
| 2021 | 6 | 167 | 0 | 1,738 |
| 2022 | 5 | 121 | 0 | 1,816 |
| 2023 | 4 | 138 | 0 | 1,720 |
| 2024 | 4 | 241 | 0 | 1,804 |
| 2025 | 0 | — | 0 | 1,890 |
| 2026 | 6 | 156 | 0 | — |
What is it indicated for?
The Artimes Balloon Dilatation Catheter is indicated for:
1. Balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis in patients evidencing coronary ischemia for the purpose of improving myocardial perfusion
2. Balloon dilatation of a coronary artery occlusion for the treatment of acute myocardial infarction
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K141025 · printed Nov 6, 2026
Cite this page
510(k) Report. “K141025: Artimes Balloon Dilatation Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141025
Report an extraction error
Are you the manufacturer?
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