# K103473: Zoll Rescuenet Epcr Model Rescuenet Epcr

- Pathway: 510(k) (Traditional)
- Applicant: ZOLL Medical Corporation
- Decided: May 13, 2011 after 170 days
- Product code: DXJ (Display, Cathode-Ray Tube, Medical)
- Device class: 2
- Regulation: 21 CFR 870.2450
- 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 K941811 (1994). 16 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100272: Intellivue Clinical Information Portfolio, Philips Medical Systems (2010) Summary page 6.

## Most influential descendants
- K132488: Zoll Code Writer (2014), 0 descendants of its own
- K131272: Siren Epcr Suite (2014), 0 descendants of its own
- K131919: Zoll Epcr Ios (2013), 0 descendants of its own

## Indications for use
RescueNet ePOR is intended for the collection, storage and printing of patient data that is entered by a user (caregiver), or captured from specified medical devices, and integrated into a patient care report (patient electronic medical record). RescueNet ePOR is intended for use by qualified medical personnel providing direct patient care in the pre-hospital environment to document the care provided. RescueNet ePOR is indicated for use by health care providers whenever there is a need for generation of a patient record.

Source page: https://510kreport.com/device/K103473
Methodology: https://510kreport.com/methodology