# Jolife AB

- Location (FDA's records): Washington, DC
- FDA decisions: 5 (2006–2018): 5 510(k) clearances
- Product codes: DRM (5)
- Predicates its devices cite: 11 (4 its own); citations of its devices by later devices: 7 (4 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Michigan Instruments, Inc.: 4 (https://510kreport.com/company/michigan-instruments)
- Revivant Corp.: 2 (https://510kreport.com/company/revivant)
- Zoll Circulation, Inc.: 1 (https://510kreport.com/company/zoll-circulation)

## Firms that cite its devices most
- Defibtech, LLC: 2 (https://510kreport.com/company/defibtech)
- Resuscitation International: 1 (https://510kreport.com/company/resuscitation-international)

## Its most-cited devices
- K090422: LUCAS 2 (2009), cited by 3
- K062401: Modification to Lucas (2006), cited by 1
- K161768: LUCAS 3 Chest Compression System (2016), cited by 1
- K173553: LUCAS 3 Chest Compression System (2018), cited by 1
- K053403: LUCAS (2006), cited by 1

## Recent decisions
- K173553: LUCAS 3 Chest Compression System (Feb 8, 2018)
- K161768: LUCAS 3 Chest Compression System (Nov 9, 2016)
- K090422: LUCAS 2 (Jun 17, 2009)
- K062401: Modification to Lucas (Sep 28, 2006)
- K053403: LUCAS (Feb 1, 2006)

Source page: https://510kreport.com/company/jolife