# K984556: Scican Classic

- Pathway: 510(k) (Traditional)
- Applicant: Scholly Fiberoptic GmbH
- Decided: Feb 9, 1999 after 48 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: 2 generations back to K933671 (1994). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981937: Welch Allyn Reveal Intraoral Camera System, Welch Allyn, Inc. (1998) Summary page 1.

## Indications for use
The SciCan Classic and accessories are indicated for use when video images are desired to provide visual information during dental examinations and procedures.

Source page: https://510kreport.com/device/K984556
Methodology: https://510kreport.com/methodology
