# Algotec Systems, Ltd.

- Location (FDA's records): Efrat, IL
- FDA decisions: 5 (1996–2003): 5 510(k) clearances
- Product codes: LLZ (5)
- Predicates its devices cite: 4 (4 its own); citations of its devices by later devices: 7 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Voxar Limited: 1 (https://510kreport.com/company/voxar)
- Intracom Corp.: 1 (https://510kreport.com/company/intracom)
- International Regulatory Consultants: 1 (https://510kreport.com/company/international-regulatory-consultants)

## Its most-cited devices
- K954678: Pro Vision (1996), cited by 2
- K980648: Pro Vision (1998), cited by 2
- K002894: Mediprime (2000), cited by 2
- K023936: Modification to Mediprime (2002), cited by 1

## Recent decisions
- K033013: Mdification to Mediprime (Nov 25, 2003)
- K023936: Modification to Mediprime (Dec 20, 2002)
- K002894: Mediprime (Dec 5, 2000)
- K980648: Pro Vision (Jul 20, 1998)
- K954678: Pro Vision (Jan 5, 1996)

Source page: https://510kreport.com/company/algotec-systems