# P190013: AED Battery Exchange (Models 9146-ABE, G5-ABE, 5070-ABE, FR3-ABE)

- Pathway: PMA
- Applicant: Aed Battery Exchange, LLC
- Decided: Feb 2, 2021 after 645 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P190013
Methodology: https://510kreport.com/methodology