# K213932: A-dec 300, A-dec 500

- Pathway: 510(k) (Traditional)
- Applicant: A-Dec, Inc.
- Decided: Mar 2, 2022 after 76 days
- Product code: EIA (Unit, Operative Dental)
- Device class: 1
- Regulation: 21 CFR 872.6640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K242404: BDC Dental Unit (2025), 0 descendants of its own

## Indications for use
The A-dec Delivery System is intended to provide a mounting location in addition to providing air, water, vacuum, and electrical power to dental devices for use during diagnostic and therapeutic treatment by licensed health care professionals. Delivery systems may be mounted to dental chairs, dental carts, dental cabinets, and walls.

Source page: https://510kreport.com/device/K213932
Methodology: https://510kreport.com/methodology