# Heartvista, Inc.

- Location (FDA's records): Los Altos, CA
- FDA decisions: 6 (2014–2021): 6 510(k) clearances
- Product codes: LNH (6)
- 510(k) review time since 2016: median 185 days, against 93 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 6 (5 its own); citations of its devices by later devices: 6 (5 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
- GE Medical Systems: 1 (https://510kreport.com/company/ge-medical-systems)

## Firms that cite its devices most
- Vista AI, Inc.: 1 (https://510kreport.com/company/vista-ai)

## Its most-cited devices
- K153740: RTHawk, HeartVista Cardiac Package (2016), cited by 1
- K183274: RTHawk, HeartVista Cardiac Package (2019), cited by 1
- K212233: RTHawk, HeartVista Cardiac Package (2021), cited by 1
- K170090: RTHawk, HeartVista Cardiac Package (2017), cited by 1
- K142997: RTHawk, HeartVista Workstation with RTHawk (2014), cited by 1
- K133848: Rthawk, Rthawk, or Heartvista Workstation with Rthawk (2014), cited by 1

## Recent decisions
- K212233: RTHawk, HeartVista Cardiac Package (Oct 5, 2021)
- K183274: RTHawk, HeartVista Cardiac Package (Oct 18, 2019)
- K170090: RTHawk, HeartVista Cardiac Package (Jul 14, 2017)
- K153740: RTHawk, HeartVista Cardiac Package (Jun 30, 2016)
- K142997: RTHawk, HeartVista Workstation with RTHawk (Dec 17, 2014)
- K133848: Rthawk, Rthawk, or Heartvista Workstation with Rthawk (Jun 25, 2014)

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