# K063602: Autopulse Resuscitation System  MODEL100

- Pathway: 510(k) (Special)
- Applicant: Zoll Circulation
- Decided: Dec 21, 2006 after 17 days
- Product code: DRM (Compressor, Cardiac, External)
- Device class: 2
- Regulation: 21 CFR 870.5200
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K851139 (1985). 5 ancestors in all.
11 later devices descend from it; 3 cite it directly.
2 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040453: Autopulse Resuscitation System, Model 100, Revivant Corp. (2004) Summary page 1.

## Most influential descendants
- K073079: Thumper, Model: 1008 (2008), 6 descendants of its own
- K090422: LUCAS 2 (2009), 5 descendants of its own
- K161768: LUCAS 3 Chest Compression System (2016), 2 descendants of its own
- K173553: LUCAS 3 Chest Compression System (2018), 1 descendant of its own
- K112998: Autopulse Resuscitation System Model 1000 (2012), 1 descendant of its own

## Recalls of this device
- Aug 8, 2012 · Class II · Z-0658-2013: Complaints associated with an unexpected stop in AutoPulse compressions.

## Indications for use
The AutoPulse Resuscitation System Model 100 is intended to be used as an adjunct to manual CPR, on adult patients only, in cases of clinical death as defined by lack of spontaneous breathing and pulse.

Source page: https://510kreport.com/device/K063602
Methodology: https://510kreport.com/methodology