# K902518: LD-Six Arterial Blood Filter for Extra. Service

- Pathway: 510(k) (Traditional)
- Applicant: Pall Biomedical Products Co.
- Decided: Oct 16, 1990 after 132 days
- Product code: DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line)
- Device class: 2
- Regulation: 21 CFR 870.4260
- Recalls of this device: 1 (0 Class I)
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K231362: OCS Heart Leukocyte Depleting Filter (2023), 0 descendants of its own

## Recalls of this device
- May 26, 2011 · Not classified · Z-2856-2011: Potential for the housing of the arterial line Leukocyte Reduction Filter to separate before or during the priming procedure.

Source page: https://510kreport.com/device/K902518
Methodology: https://510kreport.com/methodology