# Visible Patient, Sas

- Location (FDA's records): Strasbourg, FR
- FDA decisions: 2 (2015–2021): 2 510(k) clearances
- Product codes: LLZ (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 3 (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
- Fujifilm Medical Systems U.S.A, Inc.: 1 (https://510kreport.com/company/fujifilm-medical-systems-usa)
- Fujifilm Meidcal Systems U.S.A.,Inc.: 1 (https://510kreport.com/company/fujifilm-meidcal-systems-usa)
- Fujifilm Medical System U.S.A., Inc.: 1 (https://510kreport.com/company/fujifilm-medical-system-usa)

## Firms that cite its devices most
- Hutom, Inc.: 1 (https://510kreport.com/company/hutom)
- Beijing Infervision Healthcare Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/beijing-infervision-healthcare-medical-technology)

## Its most-cited devices
- K212896: Visible Patient Suite (2021), cited by 2
- K151988: Visible Patient Suite (2015), cited by 1

## Recent decisions
- K212896: Visible Patient Suite (Nov 5, 2021)
- K151988: Visible Patient Suite (Oct 15, 2015)

Source page: https://510kreport.com/company/visible-patient