# P250009: SQUID Liquid Embolic Agent (LEA)

- Pathway: PMA
- Applicant: Balt USA, LLC
- Decided: Jan 30, 2026 after 315 days
- Product code: SGU (Neurovascular Liquid Embolic Agent)
- Device class: 3
- 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. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P250009
Methodology: https://510kreport.com/methodology