# K063113: EP-Workmate

- Pathway: 510(k) (Special)
- Applicant: Ep Medsystems
- Decided: Oct 27, 2006 after 16 days
- Product code: DQK (Computer, Diagnostic, Programmable)
- Device class: 2
- Regulation: 21 CFR 870.1425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K994011 (2000). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K994011: EP Medsystems, EP-Workmate, Ep Medsystems, Inc. (2000) Summary page 1.

## Indications for use
NurseMateTM is indicated for use during clinical electrophysiology procedures.

Source page: https://510kreport.com/device/K063113
Methodology: https://510kreport.com/methodology