# K930011: Uresil Valve Cutter with Interchangeable Heads

- Pathway: 510(k) (Traditional)
- Applicant: Uresil Corp.
- Decided: May 26, 1993 after 142 days
- Product code: MGZ (Valvulotome)
- Device class: 2
- Regulation: 21 CFR 870.4885
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K190267: EZE SIT Valvulotome (2019), 0 descendants of its own
- K964061: Gore Angioscopic Valvvlotome Kit (TBD) (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K930011
Methodology: https://510kreport.com/methodology