# Aed Battery Exchange, LLC

- Location (FDA's records): Wauconda
- FDA decisions: 2 (2012–2021): 1 510(k) clearance and 1 original PMA approval
- Product codes: MKJ (2)
- Predicates its devices cite: 12 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Philips Medical Systems, Inc.: 6 (https://510kreport.com/company/philips-medical-systems)
- Cardiac Science Corporation: 2 (https://510kreport.com/company/cardiac-science)
- Defibtech, LLC: 2 (https://510kreport.com/company/defibtech)
- Heartstream, Inc.: 1 (https://510kreport.com/company/heartstream)
- Physio-Control Corp.: 1 (https://510kreport.com/company/physio-control)

## Recent decisions
- P190013: AED Battery Exchange (Models 9146-ABE, G5-ABE, 5070-ABE, FR3-ABE) (Feb 2, 2021)
- K120350: Extended Life Battery (Nov 1, 2012)

Source page: https://510kreport.com/company/aed-battery-exchange