510(k) · Cleared
Recalled · Class II · 2015Hemocor HP Hemoconcentrator Series
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Minntech Corp. · KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
Cleared on Feb 18, 1994 after a 599-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 9 later devices descend from it. It has been recalled once.
- Decided
- Feb 18, 1994
- Review
- 599 days
- Class
- Class II
- Product code
- KDI
- Recalls
- 1
- Predicates
- 0
9 later devices descend from it, 4 citing it directly.
- This deviceK923139 Hemocor HP Hemoconcentrator SeriesMinntech Corp. · 1994
- Descendant · cites it directly · 2 of its ownK021732 DHF 0.2 Hemoconcentrator: Dideco Newborn-Infant Hemoncentration; DHR…Dideco S.P.A. · 2002
- Descendant · cites it directly · 2 of its ownK973516 Capiox HemoconcentratorTerumo Medical Corp. · 1998
- Descendant · 2 generations on · 1 of its ownK081313 SH14 HemoconcentratorSorin Group Italia S.R.L. · 2008
- Descendant · cites it directly · 1 of its ownK974584 Fresenius F Series Hemoconcentrators…Fresenius USA, Inc. · 1998
- Descendant · 2 generations on · 0 of its ownK243920 Purema H Hemoconcentrator - PediatricMedica USA, Inc. · 2025
Showing 5 of 9 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 9 · See all- K021732DHF 0.2 Hemoconcentrator: Dideco Newborn-Infant Hemoncentration; DHR 0.6…Dideco S.P.A. · 2002 · cites it directly2descendants
- K973516Capiox HemoconcentratorTerumo Medical Corp. · 1998 · cites it directly2descendants
- K081313SH14 HemoconcentratorSorin Group Italia S.R.L. · 2008 · 2 generations on1descendant
- K974584Fresenius F Series Hemoconcentrators F400,F500,F700,F800,F400TS,F500TS,F700S,F800TSFresenius USA, Inc. · 1998 · cites it directly1descendant
- K243920Purema H Hemoconcentrator - PediatricMedica USA, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K923139 | Hemocor HP Hemoconcentrator Series | Minntech Corp. | 1994 | — |
| +1 | K021732 | DHF 0.2 Hemoconcentrator: Dideco Newborn-Infant Hemoncentration; DHR 0.6… | Dideco S.P.A. | 2002 | — |
| +1 | K973516 | Capiox Hemoconcentrator | Terumo Medical Corp. | 1998 | — |
| +2 | K081313 | SH14 Hemoconcentrator | Sorin Group Italia S.R.L. | 2008 | — |
| +1 | K974584 | Fresenius F Series Hemoconcentrators… | Fresenius USA, Inc. | 1998 | — |
| +2 | K243920 | Purema H Hemoconcentrator - Pediatric | Medica USA, Inc. | 2025 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 2 | 0 |
| 1999 | 1 | 0 |
| 2002 | 1 | 0 |
| 2008 | 1 | 0 |
| 2013 | 1 | 0 |
| 2024 | 1 | 0 |
| 2025 | 2 | 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 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?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (9)
4 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Aug 18, 2015 | Class II | Z-2735-2015 | Nonconforming Material/Component | Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration performance that is below product specification. These potentially affected units have been distributed as stand-alone devices and in specific lots of Medtronic… |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K021732 (Dideco S.P.A., 2002) has gone furthest, with 2 descendants of its own.
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.
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 | — |
https://510kreport.com/device/K923139 · printed Nov 6, 2026
Cite this page
510(k) Report. “K923139: Hemocor HP Hemoconcentrator Series.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K923139
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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