# Lv Liberty Vision Corporation

- Location (FDA's records): Portsmouth, NH
- FDA decisions: 2 (2017–2020): 2 510(k) clearances
- Names in FDA's records: Lv Liberty Vision Corporation (1); Lv Liberty Vision Corp. (1)
- Product codes: KXK (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
- Salutaris Medical Devices, Inc.: 1 (https://510kreport.com/company/salutaris-medical-devices)

## Its most-cited devices
- K163572: LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source (2017), cited by 1

## Recent decisions
- K193602: LV Liberty Vision Model 1 90Yttrium Brachytherapy Source (May 29, 2020)
- K163572: LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source (Mar 15, 2017)

Source page: https://510kreport.com/company/lv-liberty-vision