510(k) · Cleared
ClearedElisio-H Hemodialyzer
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Nipro Medical Corporation · KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
Cleared on Apr 14, 2014 as substantially equivalent to K131935 (Nipro Medical Corporation, 2013) and 1 other predicate after a 77-day review. Its family tree reaches back 11 generations to 2001. 1 later device descends from it.
- Decided
- Apr 14, 2014
- Review
- 77 days
- Class
- Class II
- Product code
- KDI
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 11 generations to K001283 (2001). 27 ancestors in all, the oldest K872364 (1987). 1 later device descends from it, 1 citing it directly.
- Root · 11 generations backK001283 Lifemate Hemofiltration SystemNxstage Medical, Inc. · 2001
- 7 generations between
- 3 generations backK093120 Xenium XPM 110, Xenium XPM 130, Models M25649A, M25650A, Xenium XPM…Baxter Healthcare Corporation - Renal Division · 2010
- 2 generations backK122347 Elisio-H and Elisio-M HemodialyzersNipro Medical Corporation · 2013
- 1 generation backK131381 Elisio-H HemodialyzerNipro Medical Corporation · 2013
- This deviceK140191 Elisio-H HemodialyzerNipro Medical Corporation · 2014
- Descendant · cites it directly · 0 of its ownK260533 Elisio™-HNipro Medical Corporation · 2026
Show all 11 generations
- Root · 11 generations backK001283 Lifemate Hemofiltration SystemNxstage Medical, Inc. · 2001
- 10 generations backK012510 Modification to: Lifemate Hemofiltration SystemNxstage Medical, Inc. · 2001
- 9 generations backK020858 Nxstage Therapy SystemNxstage Medical, Inc. · 2002
- 8 generations backK030470 Nxstage System OneNxstage Medical, Inc. · 2003
- 7 generations backK041424 Nxstage System OneNxstage Medical, Inc. · 2004
- 6 generations backK050525 Nxstage System OneNxstage Medical, Inc. · 2005 · Recalled
- 5 generations backK062079 Xenium Dialyzer, Models 110, 130, 150, 170, 190 and 210Baxter Healthcare Corporation · 2006
- 4 generations backK083778 Xenium XPH, Models 110, 130, 150, 170, 190 and 210Baxter Healthcare Corporation · 2009
- 3 generations backK093120 Xenium XPM 110, Xenium XPM 130, Models M25649A, M25650A, Xenium XPM…Baxter Healthcare Corporation - Renal Division · 2010
- 2 generations backK122347 Elisio-H and Elisio-M HemodialyzersNipro Medical Corporation · 2013
- 1 generation backK131381 Elisio-H HemodialyzerNipro Medical Corporation · 2013
- This deviceK140191 Elisio-H HemodialyzerNipro Medical Corporation · 2014
Most influential descendants
Showing 1 of 1 · See all- K260533Elisio™-HNipro Medical Corporation · 2026 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −11 | K001283 | Lifemate Hemofiltration System | Nxstage Medical, Inc. | 2001 | — |
| −10 | K012510 | Modification to: Lifemate Hemofiltration System | Nxstage Medical, Inc. | 2001 | — |
| −9 | K020858 | Nxstage Therapy System | Nxstage Medical, Inc. | 2002 | — |
| −8 | K030470 | Nxstage System One | Nxstage Medical, Inc. | 2003 | — |
| −7 | K041424 | Nxstage System One | Nxstage Medical, Inc. | 2004 | — |
| −6 | K050525 | Nxstage System One | Nxstage Medical, Inc. | 2005 | 2 |
| −5 | K062079 | Xenium Dialyzer, Models 110, 130, 150, 170, 190 and 210 | Baxter Healthcare Corporation | 2006 | — |
| −4 | K083778 | Xenium XPH, Models 110, 130, 150, 170, 190 and 210 | Baxter Healthcare Corporation | 2009 | — |
| −3 | K093120 | Xenium XPM 110, Xenium XPM 130, Models M25649A, M25650A, Xenium XPM 150… | Baxter Healthcare Corporation - Renal Division | 2010 | — |
| −2 | K122347 | Elisio-H and Elisio-M Hemodialyzers | Nipro Medical Corporation | 2013 | — |
| −1 | K131381 | Elisio-H Hemodialyzer | Nipro Medical Corporation | 2013 | — |
| 0 (this device) | K140191 | Elisio-H Hemodialyzer | Nipro Medical Corporation | 2014 | — |
| +1 | K260533 | Elisio™-H | Nipro Medical Corporation | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1987 | 1 | 0 |
| 1989 | 1 | 0 |
| 1991 | 1 | 0 |
| 1994 | 2 | 0 |
| 1997 | 1 | 0 |
| 1998 | 2 | 0 |
| 2000 | 1 | 0 |
| 2001 | 2 | 0 |
| 2003 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2008 | 1 | 0 |
| 2013 | 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 KDI? 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 KDI device
- #1 K243874 FX CorAL 60 (F00012969); FX CorAL 80…score 18.2 · 12 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 |
|---|---|---|---|
| * | K131935 | Elisio-H Hemodialyzer, Elisio-M HemodialyzerSummary page 1…ication High permeability hemodialysis system Name per 2ICFR 876.5860 Common Name Hemodialyzer Substantial Equivalence K131935 EL1S1OTm-H Hemodialyzer K13l381 EL1S1OTM-H Hemodialyzer Device Description The ELISIO-l-lhe… | 2013 |
| * | K131381 | Elisio-H HemodialyzerSummary page 2…y members (sizes -091-1 and -25H) are composed of polyethersulfone fiber with those of similar membrane size described in K131381. The housing case composition (polypropylene) is identical between the existing s… | 2013 |
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 |
|---|---|---|---|
| K260533 | Elisio™-H | 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 13 years and passes through 4 companies; a new generation was cleared every 12 months on median.
- 7 of the 27 ancestors have a recall of any class.
- Of its descendants, K260533 (Nipro Medical Corporation, 2026) has gone furthest, with 0 descendants of its own.
- 2 other devices also cite its predicate K131935.
How does its category compare?
All KDI devicesKDI Dialyzer, High Permeability With Or Without Sealed Dialysate System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · KDI
9in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KDI
199in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KDI
2in 2025
Class I (10 since 2007) Class II/III not classified
Adverse event reports per year · KDI
2,786in 2025
MAUDE reports naming product code KDI, 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 | 11 | 91 | 4 | 916 |
| 2008 | 6 | 148 | 0 | 1,042 |
| 2009 | 4 | 236 | 3 | 522 |
| 2010 | 9 | 186 | 1 | 823 |
| 2011 | 5 | 85 | 4 | 2,270 |
| 2012 | 6 | 153 | 1 | 1,765 |
| 2013 | 11 | 247 | 2 | 2,360 |
| 2014 | 8 | 164 | 3 | 6,154 |
| 2015 | 5 | 69 | 5 | 4,182 |
| 2016 | 5 | 230 | 4 | 766 |
| 2017 | 8 | 188 | 1 | 963 |
| 2018 | 2 | — | 1 | 1,716 |
| 2019 | 4 | 263 | 6 | 1,587 |
| 2020 | 9 | 266 | 0 | 1,633 |
| 2021 | 2 | — | 2 | 1,944 |
| 2022 | 7 | 259 | 17 | 2,180 |
| 2023 | 7 | 157 | 8 (8) | 2,692 |
| 2024 | 7 | 235 | 4 (2) | 2,441 |
| 2025 | 9 | 199 | 2 | 2,786 |
| 2026 | 6 | 154 | 2 | — |
What is it indicated for?
Hemodialysis with an EL1S1OTM-H hemodialyzer is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs.
The device is for prescription use only.
This product is intended for single use only. The performance properties of reused dialyzers have not been established.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K140191 · printed Nov 4, 2026
Cite this page
510(k) Report. “K140191: Elisio-H Hemodialyzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K140191
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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