# Intricon Datrix Corporation

- Location (FDA's records): Appollo Beach, FL
- FDA decisions: 2 (2011–2011): 2 510(k) clearances
- Product codes: DSI (1), MWJ (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (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
- Braemar, Inc.: 3 (https://510kreport.com/company/braemar)
- Datrix, Inc. Dba of Jon Barron, Inc.: 1 (https://510kreport.com/company/datrix-dba-of-jon-barron)
- Datrix: 1 (https://510kreport.com/company/datrix)

## Recent decisions
- K112601: Intricon Datrix Sirona Event/ Holter Recorder (Nov 9, 2011)
- K111160: Intricon Datrix Centauri MT Ambulatory Patient Ecg Telemetry System (Apets) (Aug 1, 2011)

Source page: https://510kreport.com/company/intricon-datrix