# K882491: Cutting Fluid System for Dental High Speed Drills

- Pathway: 510(k) (Traditional)
- Applicant: Steri-Sol, Inc.
- Decided: Aug 26, 1988 after 71 days
- Product code: EFB (Handpiece, Air-Powered, Dental)
- Device class: 1
- Regulation: 21 CFR 872.4200
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023213: RDH-2000 (2003), 0 descendants of its own
- K990479: Hygeniclear WKR 1, Water-Delivery Device Ultraclear (1999), 0 descendants of its own
- K981171: Eradic-All (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K882491
Methodology: https://510kreport.com/methodology