# K082796: Sopro 184 Camera

- Pathway: 510(k) (Traditional)
- Applicant: Sopro
- Decided: Apr 1, 2009 after 190 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: 3 generations back to K936071 (1994). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070102: Sopro 162 Camera, Sopro (2007) Summary page 1.

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

Source page: https://510kreport.com/device/K082796
Methodology: https://510kreport.com/methodology