# K091186: Kodak 1500 Intraoral Camera

- Pathway: 510(k) (Traditional)
- Applicant: Carestream Health, Inc.
- Decided: Aug 18, 2009 after 117 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
Longest line of descent: 1 generation back to K000112 (2000). 2 ancestors in all.
1 later device descends from it; 1 cites 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)
- K000112: Acucam Concept IV, Models A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401, Dentsply Intl. (2000) Summary page 2.
- K033419: STV Pro 2, Trophy Radiologie (2004) Summary page 2.

## Most influential descendants
- K111423: CS 1600 Intraoral Camera (2012), 0 descendants of its own

## Indications for use
The Kodak 1500 Intraoral Camera is indicated for use by health professionals in viewing and capturing intraoral or extraoral color video images for the purposes of: 1. Allowing practitioners to view and magnify regions of the oral cavity 2. Assisting communications with the patient by providing a view of treatment areas before and after a procedure 3. Providing images for documentation in patient records.

Source page: https://510kreport.com/device/K091186
Methodology: https://510kreport.com/methodology