# K952914: Star Technologies, Inc. Film Image Scan System

- Pathway: 510(k) (Traditional)
- Applicant: Star Technologies, Inc.
- Decided: Sep 18, 1995 after 84 days
- Product code: LMD (System, Digital Image Communications, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K972191: Digitizer Director (HSC025-01) (1997), 6 descendants of its own
- K980213: DI-2000 (1998), 5 descendants of its own
- K020243: Laserpro 16 (2002), 3 descendants of its own
- K052938: CR-PRO (2005), 2 descendants of its own
- K142718: Radlink GPS (2014), 1 descendant of its own

Source page: https://510kreport.com/device/K952914
Methodology: https://510kreport.com/methodology