# K834380: Pall EC Plus Filter

- Pathway: 510(k) (Traditional)
- Applicant: Pall Biomedical Products Co.
- Decided: Aug 3, 1984 after 233 days
- Product code: DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line)
- Device class: 2
- Regulation: 21 CFR 870.4260
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 2 cite it directly.
0 of 6 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
- K032128: Terumo AL8X Arterial Filter with X-Coating (2003), 3 descendants of its own
- K083834: Terumo Pall AL6X  Arterial Filter (2009), 1 descendant of its own
- K121209: Terumo Pall AL20X Arterial Filter (2012), 0 descendants of its own
- K083747: Terumo Pall AL3X Arterial Filter (2009), 0 descendants of its own
- K031323: DBT, Dynamic Bubble Trap (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K834380
Methodology: https://510kreport.com/methodology