# Vizaramed, Inc.

- Location (FDA's records): San Jose, CA
- FDA decisions: 2 (2022–2026): 2 510(k) clearances
- Product codes: DYB (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)

## Its most-cited devices
- K221655: Multiflex Steerable Sheath (2022), cited by 1

## Recent decisions
- K260626: Multiflex Steerable Sheath 17.5F (Mar 26, 2026)
- K221655: Multiflex Steerable Sheath (Nov 14, 2022)

Source page: https://510kreport.com/company/vizaramed