# K132073: EP-Workmate, EP-Nursemate, EP-Nursemate with Physio Module

- Pathway: 510(k) (Special)
- Applicant: St Jude Medical
- Decided: Sep 9, 2013 after 68 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: 6 generations back to K000248 (2000). 13 ancestors in all.
31 later devices descend from it; 1 cites it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092810: EP-Workmate System, Version 4.2, St Jude Medical (2009)
- K093583: EP -Nursemate, EP -Nursemate with Physio Module, St Jude Medical (2009) Summary page 1.

## Most influential descendants
- K151911: WorkMate Claris System, WorkMate Claris System Display Plus (2015), 30 descendants of its own
- K160218: AutoMark Module (2016), 28 descendants of its own
- K172396: EnSite Velocity Cardiac Mapping System v5.2 (2018), 27 descendants of its own
- K182644: EnSite Velocity Cardiac Mapping System v5.2, EnSite Precision Cardiac Mapping System v2.2 (2018), 26 descendants of its own
- K183128: EnSite Velocity Cardiac Mapping System v5.2, EnSite Precision Cardiac Mapping System v2.2 (2018), 25 descendants of its own

## Indications for use
The WorkMateTM ClarisTM System is indicated for use during clinical electrophysiology procedures.

Source page: https://510kreport.com/device/K132073
Methodology: https://510kreport.com/methodology