# Applied Cardiac Systems

- Location (FDA's records): Laguna Hills, CA
- FDA decisions: 5 (1982–2011): 5 510(k) clearances
- Names in FDA's records: Applied Cardiac Systems (4); Applied Cardiac Systems, Inc. (1)
- Product codes: DSH (2), DPS (1), DRN (1), QYX (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 4 (1 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
- Nicore Equipment & Leasing, Inc.: 2 (https://510kreport.com/company/nicore-equipment-leasing)
- Card Guard Scientific Survival, Ltd.: 2 (https://510kreport.com/company/card-guard-scientific-survival)
- Monebo Technologies, Inc.: 1 (https://510kreport.com/company/monebo-technologies)
- Memtec Corp.: 1 (https://510kreport.com/company/memtec)
- Burdick Corp.: 1 (https://510kreport.com/company/burdick)

## Firms that cite its devices most
- Pression, Inc.: 1 (https://510kreport.com/company/pression)
- Stage 2 Innovations: 1 (https://510kreport.com/company/stage-2-innovations)
- Ross Medical Technology, Inc.: 1 (https://510kreport.com/company/ross-medical-technology)

## Its most-cited devices
- K042413: Acs Model NCP-2 (2004), cited by 2
- K860249: The Holter Reporter (TM) (1986), cited by 1
- K103706: The Core (Cardiac Outpatient Realtime Ecg) Monitor (2011), cited by 1

## Recent decisions
- K103706: The Core (Cardiac Outpatient Realtime Ecg) Monitor (Aug 24, 2011)
- K042413: Acs Model NCP-2 (Dec 9, 2004)
- K860249: The Holter Reporter (TM) (Mar 11, 1986)
- K833823: Holter Performer Feather Weight/Cass (Dec 1, 1983)
- K813602: Holter Performer (Jan 29, 1982)

Source page: https://510kreport.com/company/applied-cardiac-systems