510(k) · Cleared
ClearedMaxZero Administration Sets
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Care Fusion · FPA Set, Administration, Intravascular
Cleared on Nov 20, 2014 as substantially equivalent to K051499 (Medegen Medical Manufacturing Services, 2005) and 1 other predicate after a 10-day review. Its family tree reaches back 6 generations to 1995.
- Decided
- Nov 20, 2014
- Review
- 10 days
- Class
- Class II
- Product code
- FPA
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 6 generations to K942988 (1995). 16 ancestors in all. No later device cites it as a predicate yet.
- Root · 6 generations backK942988 Filtered Extension SetsB. Braun of America, Inc. · 1995 · Recalled
- 5 generations backK955585 V2 Injection SiteB.Braun Medical, Inc. · 1996 · Recalled
- 4 generations backK973167 Positive Pressure ConnectorIcu Medical, Inc. · 1997
- 3 generations backK021692 CLC2000 Catheter Patency DeviceIcu Medical, Inc. · 2003
- 2 generations backK100434 Clave NeutronIcu Medical, Inc. · 2010 · Recalled
- 1 generation backK132413 MZ1000Care Fusion · 2013
- This deviceK143234 MaxZero Administration SetsCare Fusion · 2014
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K942988 | Filtered Extension Sets | B. Braun of America, Inc. | 1995 | 32 |
| −5 | K955585 | V2 Injection Site | B.Braun Medical, Inc. | 1996 | 27 |
| −4 | K973167 | Positive Pressure Connector | Icu Medical, Inc. | 1997 | — |
| −3 | K021692 | CLC2000 Catheter Patency Device | Icu Medical, Inc. | 2003 | — |
| −2 | K100434 | Clave Neutron | Icu Medical, Inc. | 2010 | 3 |
| −1 | K132413 | MZ1000 | Care Fusion | 2013 | — |
| 0 (this device) | K143234 | MaxZero Administration Sets | Care Fusion | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 1999 | 2 | 0 |
| 2000 | 1 | 0 |
| 2003 | 1 | 0 |
| 2005 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 1 | 0 |
| 2009 | 1 | 0 |
| 2012 | 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 FPA? 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 FPA device
- #1 K243841 Sparta Infusion Set for Insulinscore 13.4 · 3 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K051499 | Intravascular Administration Set and Extension SetSummary page 5…tial Equivalence Predicate Device Manufacturer 510(k) # Date Cleared (Primary) Medegen CareFusion (formerly K051499 June 22, 2005 Intravascular Administration Medegen) Set and Extension Set MZ1000 Needleless Connector CareFusion… | 2005 |
| * | K132413 | MZ1000Summary page 5…rmerly K051499 June 22, 2005 Intravascular Administration Medegen) Set and Extension Set MZ1000 Needleless Connector CareFusion K132413 August 29, 2013 Rational for Substantial Equivalence The information provided in the premarket notification demonstrates… | 2013 |
| † | K011193 | Nac Plus Needleless Access Connector | 2001 |
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 19 years and passes through 4 companies; a new generation was cleared every 3.1 years on median.
- 10 of the 16 ancestors have a recall of any class.
- 4 other devices also cite its predicate K051499.
How does its category compare?
All FPA devicesFPA Set, Administration, Intravascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · FPA
11in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FPA
225in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FPA
98in 2025
Class I (17 since 2007) Class II/III not classified
Adverse event reports per year · FPA
34,506in 2025
MAUDE reports naming product code FPA, 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 | 16 | 75 | 17 | 1,499 |
| 2008 | 18 | 89 | 15 | 1,941 |
| 2009 | 10 | 166 | 166 | 2,512 |
| 2010 | 23 | 120 | 58 | 2,537 |
| 2011 | 12 | 87 | 28 | 4,407 |
| 2012 | 21 | 96 | 16 (4) | 4,930 |
| 2013 | 13 | 90 | 64 | 4,651 |
| 2014 | 22 | 89 | 24 | 4,695 |
| 2015 | 17 | 123 | 6 | 6,625 |
| 2016 | 12 | 195 | 10 | 8,470 |
| 2017 | 17 | 240 | 13 | 6,462 |
| 2018 | 4 | 177 | 4 | 6,574 |
| 2019 | 7 | 161 | 13 | 11,227 |
| 2020 | 10 | 327 | 107 | 9,563 |
| 2021 | 13 | 186 | 1 | 10,414 |
| 2022 | 14 | 213 | 9 (5) | 13,393 |
| 2023 | 14 | 340 | 12 (4) | 10,916 |
| 2024 | 7 | 244 | 13 (1) | 47,210 |
| 2025 | 11 | 225 | 98 (1) | 34,506 |
| 2026 | 5 | 266 | 10 (2) | — |
What is it indicated for?
The MaxZero Intravascular Administration set with needleless connector(s) is a device used to administer fluids from a container to a patient’s vascular system. The administration set is for single patient use only. The administration set can be used for direct injection, intermittent infusion or continuous infusion.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K143234 · printed Nov 6, 2026
Cite this page
510(k) Report. “K143234: MaxZero Administration Sets.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K143234
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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