# Diagnosoft, Inc.

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 3 (2006–2011): 3 510(k) clearances
- Product codes: LNH (2), LLZ (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 7 (2 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
- Philips Medical Systems North America, Inc.: 1 (https://510kreport.com/company/philips-medical-systems-north-america)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)

## Firms that cite its devices most
- Medviso AB: 2 (https://510kreport.com/company/medviso)
- Myocardial Solutions: 1 (https://510kreport.com/company/myocardial-solutions)
- Tomtec Imaging Systems GmbH: 1 (https://510kreport.com/company/tomtec-imaging-systems)
- Marrek, Inc.: 1 (https://510kreport.com/company/marrek)

## Its most-cited devices
- K100352: Diagnosoft Harp Model 2.06 (2010), cited by 4
- K111833: Virtue (2011), cited by 2
- K061368: Diagnosoft Harp (2006), cited by 1

## Recent decisions
- K111833: Virtue (Sep 21, 2011)
- K100352: Diagnosoft Harp Model 2.06 (Mar 11, 2010)
- K061368: Diagnosoft Harp (Jul 28, 2006)

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