# K864996: Ultrasonic Scaler 3000/ Prophy-Jet 30/ Cavi-Jet 30

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply Intl.
- Decided: Feb 19, 1987 after 59 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
No predicates in its family tree.
9 later devices descend from it; 2 cite it directly.
0 of 10 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
- K970123: Dentsply Cavitron SPS Scaler System (1997), 4 descendants of its own
- K970342: Cavitron Jet with SPS System (1997), 4 descendants of its own
- K052334: Cavitron RF Ultrasonic Scaler System with Sterimate Handpiece, Model G-131 (2005), 2 descendants of its own
- K014188: New Prophy Powder (2002), 2 descendants of its own
- K021450: Clinpro Prophy Powder (2002), 1 descendant of its own

Source page: https://510kreport.com/device/K864996
Methodology: https://510kreport.com/methodology