# K021293: Arteria Blood Filter

- Pathway: 510(k) (Traditional)
- Applicant: Arteria Medical Science, Inc.
- Decided: Aug 22, 2002 after 121 days
- Product code: FPB (Filter, Infusion Line)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K993120 (1999). 1 ancestor in all.
6 later devices descend from it; 1 cites it directly.
2 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993120: Modified Blood Recipient Set, Baxter Healthcare Corp (1999) Summary page 1.

## Most influential descendants
- K083300: Gore Flow Reversal System (2009), 5 descendants of its own
- K143072: ENROUTE Transcarotid Neuroprotection System (2015), 2 descendants of its own
- K153485: ENROUTE Transcarotid Neuroprotection System (2016), 1 descendant of its own
- K230402: ENROUTE® Transcarotid Neuroprotection System (2023), 0 descendants of its own
- K123156: Gore Flow Reversal System Model GFRS073 (2012), 0 descendants of its own

## Indications for use
The ArteriA Blood Filter is intended as an accessory for use in the administration of blood, blood components or solutions into a patient’s vascular system through a venous access device.

Source page: https://510kreport.com/device/K021293
Methodology: https://510kreport.com/methodology