510(k) · Cleared
ClearedRadifocus Guide Wire M
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Terumo Medical Corp. · KOD Catheter, Urological
Cleared on Oct 2, 1992 after a 78-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 3 later devices descend from it.
- Decided
- Oct 2, 1992
- Review
- 78 days
- Class
- Class II
- Product code
- KOD
- Recalls
- None
- Predicates
- 0
3 later devices descend from it, 2 citing it directly.
- This deviceK923607 Radifocus Guide Wire MTerumo Medical Corp. · 1992
- Descendant · cites it directly · 1 of its ownK131072 Orchestra Hydrophilic Guidewire Standard Angled, Orchestra…Coloplast A/S · 2013
- Descendant · 2 generations on · 0 of its ownK150927 Orchestra Hydrophilic Guidewire standard angled, Orchestra…Coloplast A/S · 2015
- Descendant · cites it directly · 0 of its ownK060034 Nipro Hydrophilic Guidewire for Urological & Laparoscopic UseNipro Medical Corporation · 2006
Most influential descendants
Showing 3 of 3 · See all- K131072Orchestra Hydrophilic Guidewire Standard Angled, Orchestra Hydrophilic Guidewire…Coloplast A/S · 2013 · cites it directly1descendant
- K150927Orchestra Hydrophilic Guidewire standard angled, Orchestra Hydrophilic Guidewire…Coloplast A/S · 2015 · 2 generations on0descendants
- K060034Nipro Hydrophilic Guidewire for Urological & Laparoscopic UseNipro Medical Corporation · 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) | K923607 | Radifocus Guide Wire M | Terumo Medical Corp. | 1992 | — |
| +1 | K131072 | Orchestra Hydrophilic Guidewire Standard Angled, Orchestra Hydrophilic… | Coloplast A/S | 2013 | — |
| +2 | K150927 | Orchestra Hydrophilic Guidewire standard angled, Orchestra Hydrophilic… | Coloplast A/S | 2015 | — |
| +1 | K060034 | Nipro Hydrophilic Guidewire for Urological & Laparoscopic Use | Nipro Medical Corporation | 2006 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2013 | 1 | 0 |
| 2015 | 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 KOD? 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 KOD device
- #1 K251864 Rubber Utility Catheterscore 10.9 · 1 generation · 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? (3)
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?
- Of its descendants, K131072 (Coloplast A/S, 2013) has gone furthest, with 1 descendant of its own.
How does its category compare?
All KOD devicesKOD Catheter, Urological: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KOD
2in 2022
2026 to Oct 25, outlined.
Median 510(k) review, days · KOD
251in 2018
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KOD
1in 2023
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · KOD
1,389in 2025
MAUDE reports naming product code KOD, 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 | 0 | — | 0 | 180 |
| 2008 | 2 | — | 0 | 102 |
| 2009 | 1 | — | 15 | 183 |
| 2010 | 1 | — | 1 | 228 |
| 2011 | 2 | — | 47 | 209 |
| 2012 | 0 | — | 2 | 165 |
| 2013 | 0 | — | 0 | 393 |
| 2014 | 1 | — | 0 | 226 |
| 2015 | 0 | — | 0 | 418 |
| 2016 | 2 | — | 1 | 284 |
| 2017 | 1 | — | 0 | 1,873 |
| 2018 | 6 | 251 | 0 | 1,179 |
| 2019 | 1 | — | 1 | 1,167 |
| 2020 | 0 | — | 0 | 1,370 |
| 2021 | 1 | — | 0 | 1,388 |
| 2022 | 2 | — | 3 | 1,280 |
| 2023 | 0 | — | 1 (1) | 1,160 |
| 2024 | 0 | — | 0 | 1,259 |
| 2025 | 0 | — | 0 | 1,389 |
| 2026 | 1 | — | 1 | — |
https://510kreport.com/device/K923607 · printed Nov 6, 2026
Cite this page
510(k) Report. “K923607: Radifocus Guide Wire M.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K923607
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026