510(k) · Cleared
Recalled · 2004Solution Admin. Set 2C9096 W/10 PVC
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Travenol Laboratories, S.A. · FPA Set, Administration, Intravascular
Cleared on Dec 29, 1983 after a 169-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 of the 17 devices in its family, counting itself, have a Class I recall. 16 later devices descend from it. It has been recalled 2 times.
- Decided
- Dec 29, 1983
- Review
- 169 days
- Class
- Class II
- Product code
- FPA
- Recalls
- 2
- Predicates
- 0
16 later devices descend from it, 2 citing it directly. 2 of the 17 devices in this family, counting this one, have a Class I recall.
- This deviceK832284 Solution Admin. Set 2C9096 W/10 PVCTravenol Laboratories, S.A. · 1983
- Descendant · cites it directly · 14 of its ownK981792 Solution Administration SetBaxter Healthcare Corp · 1998 · Recalled
- Descendant · 2 generations on · 12 of its ownK120685 Zyno Medical Administration SetZyno Medical, LLC · 2012
- Descendant · 3 generations on · 5 of its ownK151151 U & U Intravascular Administration SetU&U Medical Technology Co, Ltd. · 2015
- Descendant · 3 generations on · 1 of its ownK232316 DEKA Infusion System, DEKA Administration SetDeka Research and Development · 2024
- Descendant · 4 generations on · 1 of its ownK230343 ProSeal™ Closed System Administration SetEpic Medical Pte., Ltd. · 2023
Showing 5 of 16 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
Most influential descendants
Showing 5 of 16 · See all- K981792Solution Administration SetBaxter Healthcare Corp · 1998 · cites it directly14descendants
- K120685Zyno Medical Administration SetZyno Medical, LLC · 2012 · 2 generations on12descendants
- K151151U & U Intravascular Administration SetU&U Medical Technology Co, Ltd. · 2015 · 3 generations on5descendants
- K232316DEKA Infusion System, DEKA Administration SetDeka Research and Development · 2024 · 3 generations on1descendant
- K230343ProSeal™ Closed System Administration SetEpic Medical Pte., Ltd. · 2023 · 4 generations on1descendant
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K832284 | Solution Admin. Set 2C9096 W/10 PVC | Travenol Laboratories, S.A. | 1983 | — |
| +1 | K981792 | Solution Administration Set | Baxter Healthcare Corp | 1998 | 5 |
| +2 | K120685 | Zyno Medical Administration Set | Zyno Medical, LLC | 2012 | — |
| +3 | K151151 | U & U Intravascular Administration Set | U&U Medical Technology Co, Ltd. | 2015 | — |
| +3 | K232316 | DEKA Infusion System, DEKA Administration Set | Deka Research and Development | 2024 | — |
| +4 | K230343 | ProSeal™ Closed System Administration Set | Epic Medical Pte., Ltd. | 2023 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
| 2012 | 1 | 0 |
| 2014 | 2 | 1 |
| 2015 | 2 | 0 |
| 2016 | 2 | 1 |
| 2018 | 1 | 0 |
| 2020 | 1 | 0 |
| 2022 | 1 | 0 |
| 2023 | 1 | 0 |
| 2024 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 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.
2 devices in this family have a Class I recall. 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?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (16)
See all 162 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (2 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Apr 28, 2004 | Not classified | Z-0193-05 | Other | Inadequate directions for use may have contributed to an increase in infection rates at a small number of customers beginning use of the Clearlink needleless device. |
| Jul 16, 2003 | Not classified | Z-1157-03 | Other | There are possible pinholes or perforations in the set tubing, caused by damage that occurred during the packaging process. |
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K153193Halo II Ambulatory Infusion System (also with trade names Nimbus II Ambulatory Infusion System, EVAA…Zyno Medical, LLC · 2016 · 3 generations on · ◆ in the 2016 descendants bar of FIG. 13 Class I recalls
- K140783Halo Ambulatory Infusion SystemZyno Medical, LLC · 2014 · 3 generations on · ◆ in the 2014 descendants bar of FIG. 12 Class I recalls
What does this lineage say?
- Of its descendants, K981792 (Baxter Healthcare Corp, 1998) has gone furthest, with 14 descendants of its own.
How does its category compare?
All FPA devicesFPA Set, Administration, Intravascular: FDA decisions, review times, recalls and adverse event reports over 20 years.
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) | — |
https://510kreport.com/device/K832284 · printed Nov 4, 2026
Cite this page
510(k) Report. “K832284: Solution Admin. Set 2C9096 W/10 PVC.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K832284
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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