# K955497: Gambro FH 22H Fiber Hemofltr/Prisma FH 22H Blood Tubing/Hemofltr Set

- Pathway: 510(k) (Traditional)
- Applicant: Cobe Renal Care, Inc.
- Decided: Sep 25, 1997 after 664 days
- Product code: KDL (Set, Perfusion, Kidney, Disposable)
- Device class: 2
- Regulation: 21 CFR 876.5880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

Source page: https://510kreport.com/device/K955497
Methodology: https://510kreport.com/methodology