# Accucore, Inc.

- Location (FDA's records): Santa Ana, CA
- FDA decisions: 9 (1987–1995): 9 510(k) clearances
- Product codes: DSI (4), DXH (3), DPS (1), DRT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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
- Invivo Research, Inc.: 2 (https://510kreport.com/company/invivo-research)
- Protocol Systems, Inc.: 1 (https://510kreport.com/company/protocol-systems)
- Trincore Systems, Inc.: 1 (https://510kreport.com/company/trincore-systems)
- Data Critical Corp.: 1 (https://510kreport.com/company/data-critical)
- Quinton, Inc.: 1 (https://510kreport.com/company/quinton)
- Johnson & Johnson Medical, Inc.: 1 (https://510kreport.com/company/johnson-johnson-medical)

## Its most-cited devices
- K942147: Pacific Communications Model 1100 (1995), cited by 4
- K925411: Model 2041-PC/ST Cardiac Telemetry Monitor (1993), cited by 2
- K913576: Datascope Model Visa Central Monitor (1992), cited by 1

## Recent decisions
- K942147: Pacific Communications Model 1100 (Jan 30, 1995)
- K925411: Model 2041-PC/ST Cardiac Telemetry Monitor (Feb 25, 1993)
- K913576: Datascope Model Visa Central Monitor (Jan 28, 1992)
- K913400: Model SCR-1000 (Aug 21, 1991)
- K896775: Pci Model 2041-B Telemetry Monitor (May 17, 1990)
- K901031: Pci Model 2041-PC Telemetry Monitor (May 17, 1990)
- K901032: Pci Model 2041-PC Telemetry Monitor W/Arrhythmia (Apr 4, 1990)
- K894340: Pci Model 2041-a Telemetry Monitor (Oct 2, 1989)

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