# K952074: Solution Set with 1.2 Micron Air Eliminating Filter

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Jul 27, 1995 after 86 days
- Product code: FPA (Set, Administration, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5440
- 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
- K161808: Solution Set with 1.2 Micron Air Eliminating Filter (2017), 0 descendants of its own

## Recalls of this device
- Aug 29, 2025 · Class II · Z-0200-2026: IV sets may leak.

Source page: https://510kreport.com/device/K952074
Methodology: https://510kreport.com/methodology