# Intrasense

- Location (FDA's records): Montpellier, FR
- FDA decisions: 3 (2007–2012): 3 510(k) clearances
- Product codes: LLZ (3)
- Predicates its devices cite: 12 (2 its own); citations of its devices by later devices: 4 (2 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
- Vital Images, Inc.: 3 (https://510kreport.com/company/vital-images)
- Pathfinder Therapeutics, Inc.: 2 (https://510kreport.com/company/pathfinder-therapeutics)
- GE Healthcare: 2 (https://510kreport.com/company/ge-healthcare)
- GE Medical Systems: 1 (https://510kreport.com/company/ge-medical-systems)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Cardiovascular Imaging Solutions, Ltd.: 1 (https://510kreport.com/company/cardiovascular-imaging-solutions)

## Firms that cite its devices most
- Keosys Sas: 1 (https://510kreport.com/company/keosys)
- Qi Imaging, LLC: 1 (https://510kreport.com/company/qi-imaging)

## Its most-cited devices
- K113620: Myrian 1.11 (2012), cited by 2
- K091001: Myrian 1.4 (2009), cited by 1
- K071000: Myrian (2007), cited by 1

## Recent decisions
- K113620: Myrian 1.11 (Jul 12, 2012)
- K091001: Myrian 1.4 (Jun 29, 2009)
- K071000: Myrian (May 14, 2007)

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