# Mediwatch, Ltd.

- Location (FDA's records): Warwickshire, GB
- FDA decisions: 2 (2003–2005): 2 510(k) clearances
- Names in FDA's records: Mediwatch, Ltd. (1); Mediwatch Plc (1)
- Product codes: IYO (2)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (0 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
- Pie Medical: 1 (https://510kreport.com/company/pie-medical)

## Firms that cite its devices most
- Mcube Technology Co., Ltd.: 1 (https://510kreport.com/company/mcube-technology)
- Signostics Pty, Ltd.: 1 (https://510kreport.com/company/signostics)

## Its most-cited devices
- K053325: Mediwatch Multiscan Ultrasound System/Scanner, Model M0002 (Scanner Only); Multiscan Ultrasound System, Model M0001 (2005), cited by 1
- K033906: Portascan Bladder Scanner, Model PA00146 (2003), cited by 1

## Recent decisions
- K053325: Mediwatch Multiscan Ultrasound System/Scanner, Model M0002 (Scanner Only); Multiscan Ultrasound System, Model M0001 (Dec 7, 2005)
- K033906: Portascan Bladder Scanner, Model PA00146 (Dec 24, 2003)

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