# K942457: Graft Thrombectomy Instruments

- Pathway: 510(k) (Traditional)
- Applicant: Intramed Laboratories, Inc.
- Decided: Feb 7, 1995 after 259 days
- Product code: MCW (Catheter, Peripheral, Atherectomy)
- Device class: 2
- Regulation: 21 CFR 870.4875
- Recalls of this device: none
- 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
- K233619: Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K942457
Methodology: https://510kreport.com/methodology