# K000112: Acucam Concept IV, Models A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply Intl.
- Decided: Apr 13, 2000 after 90 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; 2 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
- K091186: Kodak 1500 Intraoral Camera (2009), 1 descendant of its own
- K111423: CS 1600 Intraoral Camera (2012), 0 descendants of its own
- K041805: Microscope System (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K000112
Methodology: https://510kreport.com/methodology