# Danmeter A/S

- Location (FDA's records): Odense C, DK
- FDA decisions: 4 (2003–2005): 4 510(k) clearances
- Product codes: IPF (2), KPI (1), OLW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 5 (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 whose devices it cites most
- Alaris Medical Systems, Inc.: 1 (https://510kreport.com/company/alaris-medical-systems)
- Aspect Medical Systems, Inc.: 1 (https://510kreport.com/company/aspect-medical-systems)

## Firms that cite its devices most
- Otto Bock, Austria GmbH: 2 (https://510kreport.com/company/otto-bock-austria)
- Curatronic, Ltd.: 1 (https://510kreport.com/company/curatronic)
- Advantageous Medical Devices, LLC: 1 (https://510kreport.com/company/advantageous-medical-devices)
- Restorative Therapies, Inc.: 1 (https://510kreport.com/company/restorative-therapies)

## Its most-cited devices
- K032954: Elpha, Models II 500, II 1000, II 2000, II 3000 and E80 (2004), cited by 3
- K032955: Automove, Model AM800 (2003), cited by 1
- K032988: Elpha 4 Conti (2003), cited by 1

## Recent decisions
- K042315: Cerebral State Monitor - CSM (Jan 21, 2005)
- K032954: Elpha, Models II 500, II 1000, II 2000, II 3000 and E80 (Aug 9, 2004)
- K032955: Automove, Model AM800 (Dec 15, 2003)
- K032988: Elpha 4 Conti (Dec 3, 2003)

Source page: https://510kreport.com/company/danmeter-a-s