510(k) · Cleared
ClearedOSPREY PERIPHERAL IV Catheter System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Skydance Vascular, Inc. · FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Cleared on Apr 14, 2023 as substantially equivalent to K952861 (Becton Dickinson Vascular Access, Inc., 1995) after a 197-day review. Its family tree reaches back 1 generation to 1995. 2 later devices descend from it.
- Decided
- Apr 14, 2023
- Review
- 197 days
- Class
- Class II
- Product code
- FOZ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K952861 (1995). 2 later devices descend from it, 1 citing it directly.
- Root · 1 generation backK952861 Angiocath & Insyte Autoguard CathetersBecton Dickinson Vascular Access, Inc. · 1995
- This deviceK223018 OSPREY PERIPHERAL IV Catheter SystemSkydance Vascular, Inc. · 2023
- Descendant · cites it directly · 1 of its ownK231626 OSPREY Closed IV Catheter System (OspreyV2)Skydance Vascular, Inc. · 2023
- Descendant · 2 generations on · 0 of its ownK250292 OSPREY Midline Closed IV Catheter System (OspreyEDC-F20)Skydance Vascular, Inc. · 2025
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K952861 | Angiocath & Insyte Autoguard Catheters | Becton Dickinson Vascular Access, Inc. | 1995 | — |
| 0 (this device) | K223018 | OSPREY PERIPHERAL IV Catheter System | Skydance Vascular, Inc. | 2023 | — |
| +1 | K231626 | OSPREY Closed IV Catheter System (OspreyV2) | Skydance Vascular, Inc. | 2023 | — |
| +2 | K250292 | OSPREY Midline Closed IV Catheter System (OspreyEDC-F20) | Skydance Vascular, Inc. | 2025 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 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 FOZ? 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 FOZ device
- #1 K243403 BD Nexiva™ Closed IV Catheter Systemscore 14.8 · 8 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 |
|---|---|---|---|
| * | K952861 | Angiocath & Insyte Autoguard CathetersSummary page 4…fication Name: Intravascular Catheter Regulatory Class: Class II Product Code / Regulation: FOZ / 21 CFR § 880.5200 Predicate Device(s): K952861 Angiocath & Insyte Autoguard Catheters – Becton Dickinson Vascular Access inc. Indications for Use… | 1995 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K231626 | OSPREY Closed IV Catheter System (OspreyV2) | 2023 | 1 |
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 FOZ devicesFOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.
FDA decisions per year · FOZ
11in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FOZ
91in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FOZ
4in 2023
Class I (5 since 2007) Class II/III not classified
Adverse event reports per year · FOZ
5,110in 2025
MAUDE reports naming product code FOZ, 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 | 6 | 159 | 16 | 374 |
| 2008 | 9 | 103 | 0 | 422 |
| 2009 | 9 | 30 | 23 | 508 |
| 2010 | 3 | 28 | 115 | 370 |
| 2011 | 6 | 132 | 0 | 786 |
| 2012 | 13 | 122 | 0 | 560 |
| 2013 | 4 | 104 | 2 | 640 |
| 2014 | 9 | 99 | 4 | 815 |
| 2015 | 10 | 107 | 0 | 729 |
| 2016 | 9 | 63 | 3 (1) | 925 |
| 2017 | 9 | 51 | 22 | 1,966 |
| 2018 | 1 | — | 4 | 3,305 |
| 2019 | 8 | 140 | 3 | 4,365 |
| 2020 | 10 | 191 | 3 | 3,797 |
| 2021 | 4 | 242 | 1 | 4,674 |
| 2022 | 8 | 183 | 4 (2) | 4,133 |
| 2023 | 9 | 129 | 4 (2) | 4,430 |
| 2024 | 6 | 190 | 0 | 4,772 |
| 2025 | 11 | 91 | 0 | 5,110 |
| 2026 | 7 | 203 | 2 | — |
What is it indicated for?
OSPREY PERIPHERAL IV catheter is an intravascular catheter intended to be inserted into the patient’s vascular system for short-term use to sample blood, monitor blood pressure, or administer fluids intravenously.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K223018 · printed Nov 5, 2026
Cite this page
510(k) Report. “K223018: OSPREY PERIPHERAL IV Catheter System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K223018
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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