# K033962: Lad (Epiture Easytouch), Model Lad-08

- Pathway: 510(k) (Special)
- Applicant: Norwood Abbey, Ltd.
- Decided: Feb 20, 2004 after 60 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- 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. The FDA summary names its predicate without a number.
- (no number) LAD-01/06: named in the summary without a submission number

## Indications for use
LAD-08 is indicated for ablation of the outer layer of the skin prior to the application of OTC topical 4% lidocaine cream, for local dermal anesthesia.

Source page: https://510kreport.com/device/K033962
Methodology: https://510kreport.com/methodology