# K011541: Zoll Pad with CPR Aid

- Pathway: 510(k) (Traditional)
- Applicant: Zoll Medical Corp
- Decided: Apr 11, 2002 after 328 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.
24 later devices descend from it; 1 cites it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K041892: Zoll Aed Pro External Defibrillator (2005), 23 descendants of its own
- K060559: Zoll R Series Defibrillator (2006), 21 descendants of its own
- K100654: Zoll Propaq MD (2010), 11 descendants of its own
- K110742: Onestep Adult Multi-Function Electrode (2011), 9 descendants of its own
- K102468: Zoll Propaq MD (2010), 9 descendants of its own

Source page: https://510kreport.com/device/K011541
Methodology: https://510kreport.com/methodology