# Bioview, Ltd.

- Location (FDA's records): Kfar Saba, IL
- FDA decisions: 5 (2003–2014): 5 510(k) clearances
- Product codes: JOY (4), NTH (1)
- Predicates its devices cite: 19 (10 its own); citations of its devices by later devices: 18 (10 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
- Vysis: 4 (https://510kreport.com/company/vysis)
- Applied Spectral Imaging, Ltd.: 2 (https://510kreport.com/company/applied-spectral-imaging)
- Applied Imaging Corp.: 2 (https://510kreport.com/company/applied-imaging)
- Chroma Vision Medical Systems, Inc.: 1 (https://510kreport.com/company/chroma-vision-medical-systems)

## Firms that cite its devices most
- Ikonisys, Inc.: 5 (https://510kreport.com/company/ikonisys)
- Applied Spectral Imaging, Ltd.: 3 (https://510kreport.com/company/applied-spectral-imaging)

## Its most-cited devices
- K040591: Duet System (2004), cited by 6
- K050840: Modification to Duet System (2005), cited by 5
- K030192: Duet System (2003), cited by 4
- K061602: Duet System (2007), cited by 3

## Recent decisions
- K130775: Duet System (May 9, 2014)
- K061602: Duet System (Jan 23, 2007)
- K050840: Modification to Duet System (Aug 16, 2005)
- K040591: Duet System (Sep 16, 2004)
- K030192: Duet System (Aug 20, 2003)

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