# K000424: S51D Digital Endoscopy Camera

- Pathway: 510(k) (Traditional)
- Applicant: Sopro
- Decided: Mar 31, 2000 after 51 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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; 1 cites 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K031593: Sopro 61D (2003), 2 descendants of its own
- K070102: Sopro 162 Camera (2007), 1 descendant of its own
- K082796: Sopro 184 Camera (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K000424
Methodology: https://510kreport.com/methodology