# K071025: Zoll Aedpro with See-Thru CPR, Model Aedpro

- Pathway: 510(k) (Special)
- Applicant: Zoll Medical Corporation, World Wide Headquarters
- Decided: Jun 22, 2007 after 72 days
- Product code: MKJ (Automated External Defibrillators (Non-Wearable))
- Device class: 3
- Regulation: 21 CFR 870.5310
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
Use of the device for defibrillation is indicated on victims of cardiac arrest with apparent lack of circulation as indicated by: Unconsciousness Absence of breathing, and Absence of pulse and other signs of circulation When the victim is less than 8 years old or weighs less than 55 lb. (25kg), use ZOLL pedi-padz® II pediatric defibrillation electrodes. Do not delay therapy to determine the patient's exact age or weight. The device is also intended for use when ECG monitoring is indicated to evaluate the patient's heart rate or ECG morphology.

Source page: https://510kreport.com/device/K071025
Methodology: https://510kreport.com/methodology