# K072527: Autopulse Resuscitation System, Model 100

- Pathway: 510(k) (Traditional)
- Applicant: Zoll Circulation
- Decided: Mar 19, 2008 after 194 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
No predicates in its family tree.
8 later devices descend from it; 2 cite it directly.
2 of 9 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
- 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
- K221700: AutoPulse NXT Resuscitation System (2023), 0 descendants of its own

## Recalls of this device
- Jan 28, 2008 · Not classified · Z-1904-2011: Complaints of batteries discharging prematurely and that during use the Auto Pulse Units would cease operating (providing compressions).

Source page: https://510kreport.com/device/K072527
Methodology: https://510kreport.com/methodology