# K936071: Smith & Nephew Dyonics Inc. Electronic Endoscope

- Pathway: 510(k) (Traditional)
- Applicant: Smith & Nephew Dyonics, Inc.
- Decided: Aug 19, 1994 after 242 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- 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 lists a 510(k) statement for it but has not posted the file, 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/K936071
Methodology: https://510kreport.com/methodology