# K032904: Acucam Concept IV FWT, Model 110-0185G1

- Pathway: 510(k) (Special)
- Applicant: Dentsply Intl.
- Decided: Oct 14, 2003 after 27 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Gendex AcuCam Concept N Intraoral Camera System: named in the summary without a submission number
- (no number) Vistacam Omni: named in the summary without a submission number
- (no number) Vistacam Omni (IC): named in the summary without a submission number
- (no number) Ultracam: named in the summary without a submission number

## Most influential descendants
- K090079: Vivid, Models 40-A0001, 40-A0004, 40-A0006 (2009), 0 descendants of its own

## Indications for use
The AcuCam Concept IVFWTDigitalDental Intraoral Camera System is a dental imaging system intended for use by health professionals in taking intraoral and extraoral images of dental anatomy.

Source page: https://510kreport.com/device/K032904
Methodology: https://510kreport.com/methodology