510(k) · Cleared
Clearedlntravascular Administration Sets with Stopcock and Manifold
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Baxter Healthcare Corporation · FMG Stopcock, I.V. Set
Cleared on Mar 10, 2023 as substantially equivalent to K130245 (Baxter Healthcare Corp, 2013) after a 150-day review. Its family tree reaches back 2 generations to 1996.
- Decided
- Mar 10, 2023
- Review
- 150 days
- Class
- Class II
- Product code
- FMG
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K961225 (1996). 3 ancestors in all. No later device cites it as a predicate yet.
- Root · 2 generations backK961225 Continuflo Solution Set/Secondary Medication SetBaxter Healthcare Corp · 1996 · Recalled
- 1 generation backK130245 Large Bore Stopcock with Rotating Male Luer Lock/Large Bore Stopcock…Baxter Healthcare Corp · 2013 · Recalled
- This deviceK223175 lntravascular Administration Sets with Stopcock and ManifoldBaxter Healthcare Corporation · 2023
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K961225 | Continuflo Solution Set/Secondary Medication Set | Baxter Healthcare Corp | 1996 | 7 |
| −1 | K130245 | Large Bore Stopcock with Rotating Male Luer Lock/Large Bore Stopcock with… | Baxter Healthcare Corp | 2013 | 1 |
| 0 (this device) | K223175 | lntravascular Administration Sets with Stopcock and Manifold | Baxter Healthcare Corporation | 2023 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 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 FMG? 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 FMG device
- #1 K242255 Qitexio® 4-Way Stopcock (QIT014)score 10.5 · 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? (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 |
|---|---|---|---|
| * | K130245 | Large Bore Stopcock with Rotating Male Luer Lock/Large Bore Stopcock with Extension Set…Summary page 4…Table 1. Predicate Device Device Company Predicate 510(k) Clearance Date Stopcock and I.V. Baxter Healthcare K130245 (Codes: March 1, 2013 Solution Administration Corporation 2C6607 and 2C6255) Sets with Stopcocks REASON FO… | 2013 |
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 27 years and passes through 2 companies; a new generation was cleared every 16.7 years on median.
- 3 of the 3 ancestors have a recall of any class.
How does its category compare?
All FMG devicesFMG Stopcock, I.V. Set: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.
FDA decisions per year · FMG
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FMG
Too few FMG 510(k)s in any year since 2007 to give a median.
Recalls per year · FMG
33in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · FMG
868in 2025
MAUDE reports naming product code FMG, 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 | 2 | — | 5 | 26 |
| 2008 | 2 | — | 4 | 48 |
| 2009 | 2 | — | 0 | 27 |
| 2010 | 0 | — | 2 | 131 |
| 2011 | 0 | — | 8 | 95 |
| 2012 | 0 | — | 0 | 93 |
| 2013 | 2 | — | 0 | 117 |
| 2014 | 1 | — | 0 | 105 |
| 2015 | 0 | — | 0 | 96 |
| 2016 | 0 | — | 1 | 148 |
| 2017 | 0 | — | 2 | 114 |
| 2018 | 1 | — | 3 | 164 |
| 2019 | 2 | — | 0 | 400 |
| 2020 | 0 | — | 5 | 284 |
| 2021 | 0 | — | 0 | 245 |
| 2022 | 2 | — | 0 | 280 |
| 2023 | 2 | — | 0 | 689 |
| 2024 | 0 | — | 0 | 935 |
| 2025 | 1 | — | 33 (1) | 868 |
| 2026 | 0 | — | 3 | — |
What is it indicated for?
For the administration of fluids from a container into the patient's vascular system through a vascular access device.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K223175 · printed Nov 6, 2026
Cite this page
510(k) Report. “K223175: lntravascular Administration Sets with Stopcock and Manifold.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K223175
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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