# K001420: Slidescan

- Pathway: 510(k) (Traditional)
- Applicant: Applied Imaging Corp.
- Decided: Aug 30, 2000 after 117 days
- Product code: JOY (Device, Automated Cell-Locating)
- Device class: 2
- Regulation: 21 CFR 864.5260
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
14 later devices descend from it; 1 cites it directly.
0 of 15 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
- K030192: Duet System (2003), 13 descendants of its own
- K040591: Duet System (2004), 12 descendants of its own
- K050840: Modification to Duet System (2005), 7 descendants of its own
- K061602: Duet System (2007), 5 descendants of its own
- K050236: Fishview (2005), 4 descendants of its own

Source page: https://510kreport.com/device/K001420
Methodology: https://510kreport.com/methodology