510(k) · Cleared
ClearedUroject12 Syringe Lever
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Urogen Pharma, Ltd. · QBL Piston Syringe Lever
Cleared on Dec 2, 2019 as substantially equivalent to K180345 (Urogen Pharma, Ltd., 2018) after a 231-day review. Its family tree reaches back 3 generations to 1982. 1 later device descends from it.
- Decided
- Dec 2, 2019
- Review
- 231 days
- Class
- Class II
- Product code
- QBL
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K820164 (1982). 1 later device descends from it, 1 citing it directly.
- Root · 3 generations backK820164 Empty Sterile CarpujectSterling Drug, Inc. · 1982
- 2 generations backK063180 Isecure Syringe Cartridge HolderHospira, Inc. · 2006
- 1 generation backK180345 Uroject12 Syringe LeverUrogen Pharma, Ltd. · 2018
- This deviceK190987 Uroject12 Syringe LeverUrogen Pharma, Ltd. · 2019
- Descendant · cites it directly · 0 of its ownK203321 Cystoject Syringe LeverUrogen Pharma, Ltd. · 2020
Most influential descendants
Showing 1 of 1 · See all- K203321Cystoject Syringe LeverUrogen Pharma, Ltd. · 2020 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K820164 | Empty Sterile Carpuject | Sterling Drug, Inc. | 1982 | — |
| −2 | K063180 | Isecure Syringe Cartridge Holder | Hospira, Inc. | 2006 | — |
| −1 | K180345 | Uroject12 Syringe Lever | Urogen Pharma, Ltd. | 2018 | — |
| 0 (this device) | K190987 | Uroject12 Syringe Lever | Urogen Pharma, Ltd. | 2019 | — |
| +1 | K203321 | Cystoject Syringe Lever | Urogen Pharma, Ltd. | 2020 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2020 | 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 QBL? 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 QBL device
- #1 K203321 Cystoject Syringe Leverscore 1.4 · 4 generations · no Class I recall
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 |
|---|---|---|---|
| * | K180345 | Uroject12 Syringe LeverSummary page 4…0.5860 Device Class 2 III. PREDICATE DEVICE Predicate device Uroject12 Syringe Lever, by UroGen Pharma, Ltd., Product code QBL, cleared under K180345. K190987… | 2018 |
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 |
|---|---|---|---|
| K203321 | Cystoject Syringe Lever | 2020 | 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?
- The line of descent spans 37 years and passes through 3 companies; a new generation was cleared every 11.8 years on median.
- None of the 3 ancestors has a recall.
- Of its descendants, K203321 (Urogen Pharma, Ltd., 2020) has gone furthest, with 0 descendants of its own.
How does its category compare?
All QBL devicesQBL Piston Syringe Lever: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.
FDA decisions per year · QBL
1in 2020
2026 to Oct 25, outlined.
Median 510(k) review, days · QBL
Too few QBL 510(k)s in any year since 2007 to give a median.
Recalls per year · QBL
No recall names QBL since 2007.
Adverse event reports per year · QBL
2in 2023
MAUDE reports naming product code QBL, 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 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 1 | — | 0 | 0 |
| 2020 | 1 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Uroject12 Syringe Lever Device is intended for use in the administration of sterile materials under aseptic conditions, in a clinical urology setting, by a clinician and in accordance with the best judgment of a physician.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K190987 · printed Nov 4, 2026
Cite this page
510(k) Report. “K190987: Uroject12 Syringe Lever.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K190987
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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