510(k) · Cleared
ClearedCatheter, Argyle Thoracic
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sherwood Medical Industries · DWS Instruments, Surgical, Cardiovascular
Cleared on Aug 23, 1976 after a 21-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.
- Decided
- Aug 23, 1976
- Review
- 21 days
- Class
- Class I
- Product code
- DWS
- Recalls
- None
- Predicates
- 0
1 later device descends from it, 1 citing it directly.
- This deviceK760351 Catheter, Argyle ThoracicSherwood Medical Industries · 1976
- Descendant · cites it directly · 0 of its ownK971023 Chase Thoracic CatheterChase Medical, Inc. · 1997
Most influential descendants
Showing 1 of 1 · See all- K971023Chase Thoracic CatheterChase Medical, Inc. · 1997 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K760351 | Catheter, Argyle Thoracic | Sherwood Medical Industries | 1976 | — |
| +1 | K971023 | Chase Thoracic Catheter | Chase Medical, Inc. | 1997 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 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 DWS? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin 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? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K971023 | Chase Thoracic Catheter | 1997 | 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?
- Of its descendants, K971023 (Chase Medical, Inc., 1997) has gone furthest, with 0 descendants of its own.
How does its category compare?
All DWS devicesDWS Instruments, Surgical, Cardiovascular: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · DWS
FDA has decided no DWS device since 2007.
Median 510(k) review, days · DWS
Too few DWS 510(k)s in any year since 2007 to give a median.
Recalls per year · DWS
1in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DWS
12in 2025
MAUDE reports naming product code DWS, 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 | 20 |
| 2008 | 0 | — | 0 | 15 |
| 2009 | 0 | — | 0 | 44 |
| 2010 | 0 | — | 1 | 27 |
| 2011 | 0 | — | 1 | 55 |
| 2012 | 0 | — | 0 | 33 |
| 2013 | 0 | — | 0 | 34 |
| 2014 | 0 | — | 0 | 43 |
| 2015 | 0 | — | 0 | 26 |
| 2016 | 0 | — | 1 | 33 |
| 2017 | 0 | — | 0 | 40 |
| 2018 | 0 | — | 0 | 60 |
| 2019 | 0 | — | 0 | 28 |
| 2020 | 0 | — | 0 | 28 |
| 2021 | 0 | — | 0 | 32 |
| 2022 | 0 | — | 1 | 35 |
| 2023 | 0 | — | 0 | 18 |
| 2024 | 0 | — | 0 | 48 |
| 2025 | 0 | — | 0 | 12 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K760351 · printed Nov 6, 2026
Cite this page
510(k) Report. “K760351: Catheter, Argyle Thoracic.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K760351
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026