# K150349: Rapid Hair Removal Pads

- Pathway: 510(k) (Traditional)
- Applicant: Full Power Aed
- Decided: Jul 14, 2015 after 153 days
- Product code: LDD (Dc-Defibrillator, Low-Energy, (Including Paddles))
- Device class: 2
- Regulation: 21 CFR 870.5300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K964469 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
1 of 2 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K964469: 700-F Series Stimulation Electrodes, Cardiotronics Systems, Inc. (1996) Summary page 4.

## Indications for use
To remove excessive hair prior to placement of defibrillator electrodes.

Source page: https://510kreport.com/device/K150349
Methodology: https://510kreport.com/methodology