# K914790: Hollow Fiber Dialyzer Focus 9OR/90H-R/120R/120H-R

- Pathway: 510(k) (Traditional)
- Applicant: National Medical Care, Medical Products Div., Inc.
- Decided: Mar 5, 1993 after 499 days
- Product code: FJI (Dialyzer, Capillary, Hollow Fiber)
- Device class: 2
- Regulation: 21 CFR 876.5820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K990159: Dynamic Hollow Fiber Dialyzer DH-Series, Model AH 90111 (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K914790
Methodology: https://510kreport.com/methodology