# K171150: AW-100

- Pathway: 510(k) (Traditional)
- Applicant: Micron Corporation
- Decided: Mar 8, 2018 after 323 days
- Product code: ELC (Scaler, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 872.4850
- 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 K081268 (2009). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081268: Sonic Air MM1500 + (Mid), Model 50400014, Micro-Mega Societe Anonyme (2009) Summary page 4.

## Indications for use
The device is intended to be used for endodontics (canal preparation and canal cleaning).

Source page: https://510kreport.com/device/K171150
Methodology: https://510kreport.com/methodology