# P200007: HeartSync Multifunction Disposable Single-Use AED Defibrillator Pads

- Pathway: PMA
- Applicant: Graphic Controls D.B.A. Vermed
- Decided: Jun 23, 2023 after 1,236 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/P200007
Methodology: https://510kreport.com/methodology