# Seismed Instruments, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 3 (1989–1992): 3 510(k) clearances
- Product codes: DSB (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Heartforce Medical, Inc.: 1 (https://510kreport.com/company/heartforce-medical)

## Its most-cited devices
- K910994: Modified Seismocardiograph (1992), cited by 1

## Recent decisions
- K910994: Modified Seismocardiograph (Jan 15, 1992)
- K900130: Modified Seismocardiograph (Mar 28, 1990)
- K892323: Seismocardiograph - SCG (TM) 1000 Series (Oct 30, 1989)

Source page: https://510kreport.com/company/seismed-instruments