# Brainmaster

- Location (FDA's records): Great Neck, NY
- FDA decisions: 1 (1999–1999): 1 510(k) clearance
- Product codes: HCC (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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
- Lexicor Medical Technology, Inc.: 1 (https://510kreport.com/company/lexicor-medical-technology)
- Stoelting Co.: 1 (https://510kreport.com/company/stoelting)

## Firms that cite its devices most
- Eeg Software, LLC: 1 (https://510kreport.com/company/eeg-software)
- Corscience GmbH & Co. KG: 1 (https://510kreport.com/company/corscience)
- Iasis Technologies: 1 (https://510kreport.com/company/iasis-technologies)

## Its most-cited devices
- K990538: Brainmaster 2E Module and Software Biofeedback Device (1999), cited by 3

## Recent decisions
- K990538: Brainmaster 2E Module and Software Biofeedback Device (May 19, 1999)

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