# K240460: FMD Peripheral Guide Wire F-18 Flex 400 (CSU415400259)

- Pathway: 510(k) (Special)
- Applicant: FMD Co., Ltd.
- Decided: Jun 13, 2024 after 118 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- 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. FDA’s summary for it could not be read, so its predicates are not known.

Source page: https://510kreport.com/device/K240460
Methodology: https://510kreport.com/methodology