# K981663: Digital Doc

- Pathway: 510(k) (Traditional)
- Applicant: Digital Doc, LLC
- Decided: Aug 10, 1998 after 91 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K032341: Intra Oral Camera System and Accessories, Model Claris I310 (2003), 1 descendant of its own
- K061175: Claris I310D Intraoral Camera System & Accessories (2006), 0 descendants of its own
- K040691: Intra Oral Camera System & Accessories, Model Win-100D (2004), 0 descendants of its own

## Indications for use
The intraoral camera system, Digital Doc, of Digital Doc, Inc. is used to provide a view of the mouth in order to assist the dentist in describing dental procedureé and to show a patient before and after views of his mouth showing the patient results of the dental procedures which the dentist has performed on him.

Source page: https://510kreport.com/device/K981663
Methodology: https://510kreport.com/methodology