# K070102: Sopro 162 Camera

- Pathway: 510(k) (Traditional)
- Applicant: Sopro
- Decided: Feb 20, 2007 after 41 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
Longest line of descent: 2 generations back to K936071 (1994). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031593: Sopro 61D, Sopro (2003) Summary page 1.

## Most influential descendants
- K082796: Sopro 184 Camera (2009), 0 descendants of its own

## Indications for use
Providing access, illumination and allow observation or manipulation of body cavities, hollow organs, and canals.

Source page: https://510kreport.com/device/K070102
Methodology: https://510kreport.com/methodology