# Braemar Manufacturing, LLC

- Location (FDA's records): San Diego, CA
- FDA decisions: 3 (2013–2018): 3 510(k) clearances
- Product codes: MWJ (1), DSI (1), DSH (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 4 (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
- Dms-Service, LLC: 2 (https://510kreport.com/company/dms-service)
- Braemar, Inc.: 1 (https://510kreport.com/company/braemar)
- Cardionet, Inc.: 1 (https://510kreport.com/company/cardionet)

## Firms that cite its devices most
- Infobionic, Inc.: 1 (https://510kreport.com/company/infobionic)
- Wellysis Corp.: 1 (https://510kreport.com/company/wellysis)
- Biotricity: 1 (https://510kreport.com/company/biotricity)
- Smwmed, Inc.: 1 (https://510kreport.com/company/smwmed)

## Its most-cited devices
- K171410: ePatch (2018), cited by 3
- K153473: Braemar Telemetry Patch System (2016), cited by 1

## Recent decisions
- K171410: ePatch (Jan 4, 2018)
- K153473: Braemar Telemetry Patch System (Jul 22, 2016)
- K130294: Braemar Cardiokey Holter Recorder (Oct 16, 2013)

Source page: https://510kreport.com/company/braemar-manufacturing