# Moberg Medical, Inc.

- Location (FDA's records): Ambler, PA
- FDA decisions: 2 (1992–1996): 2 510(k) clearances
- Product codes: GWQ (1), GWF (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 6 (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
- Nihon Kohden America, Inc.: 1 (https://510kreport.com/company/nihon-kohden-america)

## Firms that cite its devices most
- Astro-Med, Inc.: 2 (https://510kreport.com/company/astro-med)
- Moberg Research, Inc.: 1 (https://510kreport.com/company/moberg-research)
- Axon Systems, Inc.: 1 (https://510kreport.com/company/axon-systems)
- Hewlett-Packard Co.: 1 (https://510kreport.com/company/hewlett-packard)

## Its most-cited devices
- K914571: Neurotrac II (1992), cited by 4
- K960170: Electroencephalograph (Eeg) (1996), cited by 2

## Recent decisions
- K960170: Electroencephalograph (Eeg) (Mar 1, 1996)
- K914571: Neurotrac II (Jan 30, 1992)

Source page: https://510kreport.com/company/moberg-medical