# K934783: Kavo Intrasept 905

- Pathway: 510(k) (Traditional)
- Applicant: Kavo America
- Decided: May 16, 1994 after 222 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K984244: Orl-E-92 Surgical Drill System (1999), 1 descendant of its own
- K031540: Apex Electric Handpiece System (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K934783
Methodology: https://510kreport.com/methodology