# Bodyvision Medical, Ltd.

- Location (FDA's records): Ramat Hasharon, IL
- FDA decisions: 4 (2017–2024): 4 510(k) clearances
- Product codes: LLZ (2), EOQ (1), QIH (1)
- 510(k) review time since 2016: median 160 days, against 124 for FDA's reviews in the same codes and years (0 of 4 faster)
- Predicates its devices cite: 3 (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
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)

## Firms that cite its devices most
- Novarad Corporation: 1 (https://510kreport.com/company/novarad)
- Serpex Medical, Inc.: 1 (https://510kreport.com/company/serpex-medical)

## Its most-cited devices
- K172955: LungVision Tool (2018), cited by 1
- K183593: Lung Vision System (2019), cited by 1
- K163622: Lung Vision (2017), cited by 1

## Recent decisions
- K240943: LungVision (Oct 1, 2024)
- K183593: Lung Vision System (Apr 18, 2019)
- K172955: LungVision Tool (Apr 26, 2018)
- K163622: Lung Vision (May 11, 2017)

Source page: https://510kreport.com/company/bodyvision-medical