# Cerebrotech Medical Systems, Inc.

- Location (FDA's records): Pleasanton, CA
- FDA decisions: 2 (2017–2018): 2 510(k) clearances
- Names in FDA's records: Cerebrotech Medical Systems, Inc. (1); Cerebrotech Medical Systems (1)
- Product codes: QAF (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (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
- ImpediMed Limited: 1 (https://510kreport.com/company/impedimed)

## Firms that cite its devices most
- Stroke DX: 1 (https://510kreport.com/company/stroke-dx)

## Its most-cited devices
- K182967: Visor System (2018), cited by 1
- K171186: Cerebrotech CMS-5000 (2017), cited by 1

## Recent decisions
- K182967: Visor System (Nov 23, 2018)
- K171186: Cerebrotech CMS-5000 (Dec 8, 2017)

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