# Ep Medsystems

- Location (FDA's records): West Berlin, NJ
- FDA decisions: 15 (1996–2009): 15 510(k) clearances
- Names in FDA's records: Ep Medsystems (12); Ep Medsystems, Inc. (3)
- Product codes: DQK (5), DRF (3), JOQ (3), IYN (2), DYB (1), ITN (1)
- Predicates its devices cite: 16 (7 its own); citations of its devices by later devices: 13 (7 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biosense Webster, Inc.: 8 (https://510kreport.com/company/biosense-webster)
- Biosense, Ltd.: 1 (https://510kreport.com/company/biosense)

## Firms that cite its devices most
- Zonare Medical Systems, Inc.: 2 (https://510kreport.com/company/zonare-medical-systems)
- Cardio-Optics, Inc.: 1 (https://510kreport.com/company/cardio-optics)
- Envisioneering, LLC: 1 (https://510kreport.com/company/envisioneering)
- Philips Ultrasound, Inc.: 1 (https://510kreport.com/company/philips-ultrasound)
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)

## Its most-cited devices
- K031066: Viewmate Ultrasound Imaging System (2003), cited by 5
- K994011: EP Medsystems, EP-Workmate (2000), cited by 3
- K033963: EP Deflectable Catheters (2004), cited by 1
- K063277: Mapmate (2006), cited by 1
- K071028: Viewmate System (2007), cited by 1
- K073709: Modification to Viewmate System (2008), cited by 1

## Recent decisions
- K092913: EP-4TM Cardiac Stimulator, Models: EP-04-02, EP-04-04 (Oct 16, 2009)
- K073709: Modification to Viewmate System (Mar 11, 2008)
- K071028: Viewmate System (May 1, 2007)
- K070706: EP-Workmate (Apr 11, 2007)
- K063277: Mapmate (Nov 30, 2006)
- K063113: EP-Workmate (Oct 27, 2006)
- K041442: EP-4 Clinical Stimutator (Sep 14, 2004)
- K033963: EP Deflectable Catheters (Apr 15, 2004)

Source page: https://510kreport.com/company/ep-medsystems