# Cruzar Medsystems, Inc.

- Location (FDA's records): Braintree, MA
- FDA decisions: 2 (2015–2022): 2 510(k) clearances
- Product codes: DQY (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
- Endocross, Ltd.: 1 (https://510kreport.com/company/endocross)

## Its most-cited devices
- K151896: Houdini Catheter (2015), cited by 1

## Recent decisions
- K213466: Houdini Cross Support Catheter (Oct 20, 2022)
- K151896: Houdini Catheter (Dec 7, 2015)

Source page: https://510kreport.com/company/cruzar-medsystems