# Epiep, Inc.

- Location (FDA's records): New Haven, CT
- FDA decisions: 2 (2014–2017): 2 510(k) clearances
- Product codes: DYB (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (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
- St. Jude Medical, Cardiac Rhythm Management Divisi: 1 (https://510kreport.com/company/st-jude-medical-cardiac-rhythm-management-divisi)
- Mirador Biomedical, Inc.: 1 (https://510kreport.com/company/mirador-biomedical)

## Its most-cited devices
- K142245: EpiAccess System (2014), cited by 1

## Recent decisions
- K170831: EpiAccess System (May 9, 2017)
- K142245: EpiAccess System (Oct 29, 2014)

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