510(k) · Cleared
ClearedVitajet
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Vitajet Corp. · KZE Injector, Fluid, Non-Electrically Powered
Cleared on Dec 10, 1996 after a 158-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 4 later devices descend from it.
- Decided
- Dec 10, 1996
- Review
- 158 days
- Class
- Class II
- Product code
- KZE
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 1 citing it directly.
- This deviceK962625 VitajetVitajet Corp. · 1996
- Descendant · cites it directly · 3 of its ownK994384 ClickerBioject, Inc. · 2000
- Descendant · 2 generations on · 1 of its ownK050734 Cool.ClickBioject, Inc. · 2005
- Descendant · 2 generations on · 0 of its ownK060819 Cool.Click 2Medical House Products Limited · 2006
- Descendant · 2 generations on · 0 of its ownK024018 Avant Guardian 101Avant Medical Corporation · 2003
Most influential descendants
Showing 4 of 4 · See all- K994384ClickerBioject, Inc. · 2000 · cites it directly3descendants
- K050734Cool.ClickBioject, Inc. · 2005 · 2 generations on1descendant
- K060819Cool.Click 2Medical House Products Limited · 2006 · 2 generations on0descendants
- K024018Avant Guardian 101Avant Medical Corporation · 2003 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K962625 | Vitajet | Vitajet Corp. | 1996 | — |
| +1 | K994384 | Clicker | Bioject, Inc. | 2000 | — |
| +2 | K050734 | Cool.Click | Bioject, Inc. | 2005 | — |
| +2 | K060819 | Cool.Click 2 | Medical House Products Limited | 2006 | — |
| +2 | K024018 | Avant Guardian 101 | Avant Medical Corporation | 2003 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 1 | 0 |
| 2003 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 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 KZE? 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K994384 | Clicker | 2000 | 3 |
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, K994384 (Bioject, Inc., 2000) has gone furthest, with 3 descendants of its own.
How does its category compare?
All KZE devicesKZE Injector, Fluid, Non-Electrically Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KZE
1in 2012
2026 to Oct 25, outlined.
Median 510(k) review, days · KZE
220in 2009
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KZE
1in 2010
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KZE
1in 2025
MAUDE reports naming product code KZE, 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 | 54 |
| 2008 | 0 | — | 0 | 5 |
| 2009 | 4 | 220 | 0 | 8 |
| 2010 | 0 | — | 1 | 9 |
| 2011 | 2 | — | 0 | 7 |
| 2012 | 1 | — | 0 | 6 |
| 2013 | 0 | — | 0 | 4 |
| 2014 | 0 | — | 0 | 10 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 1 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 1 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 1 |
| 2025 | 0 | — | 0 | 1 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K962625 · printed Nov 4, 2026
Cite this page
510(k) Report. “K962625: Vitajet.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K962625
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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