# Endovascular Instruments, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 1 (1998–1998): 1 510(k) clearance
- Product codes: DRE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Vascumetrix, LLC: 1 (https://510kreport.com/company/vascumetrix)

## Its most-cited devices
- K974617: Peripheral Vascular Dilator (1998), cited by 1

## Recent decisions
- K974617: Peripheral Vascular Dilator (Dec 1, 1998)

Source page: https://510kreport.com/company/endovascular-instruments