# K962665: A-Dec Self-Contained Water System

- Pathway: 510(k) (Traditional)
- Applicant: A-Dec, Inc.
- Decided: Aug 22, 1996 after 44 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.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K023815: C-1805M (2003), 0 descendants of its own
- K023896: C-1890 (2003), 0 descendants of its own
- K023213: RDH-2000 (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K962665
Methodology: https://510kreport.com/methodology