# K980859: Hemocor HPH Mini Hemoconcentrator

- Pathway: 510(k) (Traditional)
- Applicant: Minntech Corp.
- Decided: May 12, 1998 after 68 days
- Product code: KDI (Dialyzer, High Permeability With Or Without Sealed Dialysate System)
- Device class: 2
- Regulation: 21 CFR 876.5860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Hemocor HPH® 400 Hemoconcentrator: named in the summary without a submission number

## Most influential descendants
- K050952: HPH Junior High Performance Hemoconcentrator (2006), 2 descendants of its own
- K071298: HF Junior Hemofilter (2007), 1 descendant of its own
- K123395: Nxstage System One Low Volume Cartridge Express (2013), 0 descendants of its own

## Indications for use
The Hemocor HPH Mini Hemoconcentrator is intended for the relief or mitigation of overhydration, reduction of lower molecular weight constituents and to increase formed cellular elements and protein levels in the blood of patients during and/or after cardiopulmonary procedures.

Source page: https://510kreport.com/device/K980859
Methodology: https://510kreport.com/methodology