# Neurotron, Inc.

- Location (FDA's records): Baltimore, MD
- FDA decisions: 2 (1985–1986): 2 510(k) clearances
- Product codes: LLN (1), JXE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (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
- Neuro-Diagnostic Assoc.: 2 (https://510kreport.com/company/neuro-diagnostic-assoc)
- Osachi Co., Ltd.: 1 (https://510kreport.com/company/osachi)
- Neurometrix, Inc.: 1 (https://510kreport.com/company/neurometrix)
- Mde Orvosbiológiai Kutató, Fejleszto,: 1 (https://510kreport.com/company/mde-orvosbiologiai-kutato-fejleszto)
- Neurotron Medical: 1 (https://510kreport.com/company/neurotron-medical)

## Its most-cited devices
- K853608: Neurometer (1986), cited by 4
- K843924: Digital Electroneurometer S-100 (1985), cited by 2

## Recent decisions
- K853608: Neurometer (Jun 12, 1986)
- K843924: Digital Electroneurometer S-100 (Mar 12, 1985)

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