# K122200: A3F Frational

- Pathway: 510(k) (Traditional)
- Applicant: Pollogen, Ltd.
- Decided: Apr 18, 2013 after 267 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K943450 (1995). 224 ancestors in all.
No later device cites it as a predicate yet.
0 of 225 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073572: Matrix RF Applicator, Syneron Medical, Ltd. (2008) Summary page 2.

## Indications for use
The Applicator 3 Fractional (A3F) is intended for dermatological procedures requiring ablation and resurfacing of the skin

Source page: https://510kreport.com/device/K122200
Methodology: https://510kreport.com/methodology