# K103579: Intra Skan DC

- Pathway: 510(k) (Traditional)
- Applicant: Skanray Technologies
- Decided: Mar 18, 2011 after 102 days
- Product code: EHD (Unit, X-Ray, Extraoral With Timer)
- Device class: 2
- Regulation: 21 CFR 872.1800
- 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 K935046 (1994). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043092: Preva, 76IN Arm, 66IN Arm, 56IN Arm, Models P7017, P7016, P7015, Progeny, Inc. (2004) Summary page 1.
- K935046: GX-770 X-Ray Control, Model 46-404600G4, Gendex Corp. (1994)
- K992610: Gendex 765DC, Model 110-0154, Dentsply Intl. (1999) Summary page 1.

## Most influential descendants
- K111330: Air Techniques High Frequency Intra-Oral X-Ray (2011), 1 descendant of its own
- K170967: Intraskan DC Plus (2017), 0 descendants of its own

## Indications for use
The INTRA SKAN DC Intraoral Dental X-Ray System is to be used as an extraoral source of X-Rays in Dental radiography.

Source page: https://510kreport.com/device/K103579
Methodology: https://510kreport.com/methodology