# Kardium, Inc.

- Location (FDA's records): Burnaby, CA
- FDA decisions: 3 (2025–2025): 2 510(k) clearances and 1 original PMA approval
- Product codes: QZI (1), DRA (1), DQK (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Recent decisions
- P240044: Globe® Pulsed Field System (Aug 27, 2025)
- K250747: Globe® Pulsed Field System (Jun 25, 2025)
- K250529: Globe Introducer (601-01001) (Jun 3, 2025)

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