510(k) · Cleared
ClearedEmpty EVA Bag
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Haemotronic S.P.A. · KPE Container, I.V.
Cleared on Aug 19, 2021 as substantially equivalent to K193528 (Haemotronic S.P.A., 2020) after a 160-day review. Its family tree reaches back 5 generations to 1995. 1 later device descends from it.
- Decided
- Aug 19, 2021
- Review
- 160 days
- Class
- Class II
- Product code
- KPE
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 5 generations to K945193 (1995). 9 ancestors in all, the oldest K911567 (1991). 1 later device descends from it, 1 citing it directly.
- Root · 5 generations backK945193 All-in-One Two Chamber ContainerBaxter Healthcare Corp · 1995
- 4 generations backK020485 All-in-One Two Chamber Container 3200 ML, 2000 ML & 1000 MLBaxter Healthcare Corp · 2002
- 3 generations backK041038 Churchill Medical Dual Chamber Empty ContainerChurchill Medical Systems, Inc. · 2004
- 2 generations backK121161 Empty Eva Solution Container Empty Eva Dual Chamber Solution ContainerActa Medical, LLC · 2012
- 1 generation backK193528 Empty EVA BagHaemotronic S.P.A. · 2020
- This deviceK210749 Empty EVA BagHaemotronic S.P.A. · 2021
- Descendant · cites it directly · 0 of its ownK251139 KabiHelp® Uno; KabiHelp® Advance plusFresenius Kabi AG · 2026
Most influential descendants
Showing 1 of 1 · See all- K251139KabiHelp® Uno; KabiHelp® Advance plusFresenius Kabi AG · 2026 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K945193 | All-in-One Two Chamber Container | Baxter Healthcare Corp | 1995 | — |
| −4 | K020485 | All-in-One Two Chamber Container 3200 ML, 2000 ML & 1000 ML | Baxter Healthcare Corp | 2002 | — |
| −3 | K041038 | Churchill Medical Dual Chamber Empty Container | Churchill Medical Systems, Inc. | 2004 | — |
| −2 | K121161 | Empty Eva Solution Container Empty Eva Dual Chamber Solution Container | Acta Medical, LLC | 2012 | — |
| −1 | K193528 | Empty EVA Bag | Haemotronic S.P.A. | 2020 | — |
| 0 (this device) | K210749 | Empty EVA Bag | Haemotronic S.P.A. | 2021 | — |
| +1 | K251139 | KabiHelp® Uno; KabiHelp® Advance plus | Fresenius Kabi AG | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1991 | 1 | 0 |
| 1996 | 1 | 0 |
| 1997 | 1 | 0 |
| 2003 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2026 | 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 KPE? 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 KPE device
- #1 K223674 eZSURE™ Empty Fluid Container (models 426030…score 13.1 · 5 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 |
|---|---|---|---|
| * | K193528 | Empty EVA BagSummary page 4…General Hospital PREDICATE DEVICES: Manufacturer: Haemotronic S.p.a. Trade Name: Empty EVA Bag 510(k): K193528 DEVICE DESCRIPTION: The product is an empty flexible container (bag) in plastic material, that is to be filled before use… | 2020 |
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 |
|---|---|---|---|
| K251139 | KabiHelp® Uno; KabiHelp® Advance plus | 2026 | 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 26 years and passes through 4 companies; a new generation was cleared every 6.8 years on median.
- 2 of the 9 ancestors have a recall of any class.
- Of its descendants, K251139 (Fresenius Kabi AG, 2026) has gone furthest, with 0 descendants of its own.
How does its category compare?
All KPE devicesKPE Container, I.V.: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.
FDA decisions per year · KPE
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KPE
183in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KPE
16in 2024
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · KPE
220in 2025
MAUDE reports naming product code KPE, 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 | 43 |
| 2008 | 1 | — | 0 | 22 |
| 2009 | 1 | — | 3 | 38 |
| 2010 | 0 | — | 14 | 87 |
| 2011 | 2 | — | 0 | 797 |
| 2012 | 1 | — | 0 | 1,229 |
| 2013 | 1 | — | 0 | 622 |
| 2014 | 0 | — | 2 (2) | 575 |
| 2015 | 0 | — | 0 | 543 |
| 2016 | 0 | — | 0 | 527 |
| 2017 | 0 | — | 1 | 284 |
| 2018 | 0 | — | 13 | 142 |
| 2019 | 3 | 183 | 0 | 205 |
| 2020 | 1 | — | 0 | 147 |
| 2021 | 2 | — | 0 | 162 |
| 2022 | 0 | — | 2 | 112 |
| 2023 | 2 | — | 0 | 127 |
| 2024 | 1 | — | 16 | 158 |
| 2025 | 2 | — | 0 | 220 |
| 2026 | 3 | 270 | 0 | — |
What is it indicated for?
The Empty EVA Bag is an empty container used for administration of solutions to the patients using an intravascular administration set. Medication transfer in and out of the container is done using aseptic technique.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K210749 · printed Nov 4, 2026
Cite this page
510(k) Report. “K210749: Empty EVA Bag.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K210749
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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