# Digisonics, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 3 (1980–1997): 3 510(k) clearances
- Product codes: HEM (1), LLZ (1), DQK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Cone Instruments, Inc.: 1 (https://510kreport.com/company/cone-instruments)
- Vision Chips, Inc.: 1 (https://510kreport.com/company/vision-chips)
- AS Software, LLC: 1 (https://510kreport.com/company/as-software)

## Its most-cited devices
- K970402: Doctors Review System (1997), cited by 2
- K800766: Echo-Comp (1980), cited by 1

## Recent decisions
- K970402: Doctors Review System (Mar 26, 1997)
- K900271: Model OB-500 Fetal Growth Analysis & Option Oblink (Apr 19, 1990)
- K800766: Echo-Comp (Apr 24, 1980)

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