# K031379: Dyonics Vision 325Z DV3-CCD Hermes Ready Camera System, Model 7209531

- Pathway: 510(k) (Special)
- Applicant: Smith & Nephew, Inc.
- Decided: May 22, 2003 after 21 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.
10 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Images Digital 3-Chip Color Video Camera: named in the summary without a submission number

## Most influential descendants
- K070266: 560 High Definition Camera System (2007), 9 descendants of its own
- K101734: Visionscope High Definition Endoscopy Camera System with; Camera Control Unit; Camera Handpiece; Visionscope Endoscopes (2010), 7 descendants of its own
- K153606: LENS Camera Control Unit-WiFi, LENS Camera Unit-Non-WiFi, LENS camera head, Camera Coupler, Tablet Application (2016), 6 descendants of its own
- K190367: Smith & Nephew Tablet Application (2019), 3 descendants of its own
- K192876: INTELLIO Tablet Application (2020), 2 descendants of its own

## Indications for use
The Smith & Nephew DyonicsQ Vision 3252 DV 3-CCD Color Video Camera System is indicated for use in endoscopic surgical procedures to allow visualization of the articular cavities, body cavities, hollow organs and canals, when used with an appropriately indicated endoscope. Additionally, when used in conjunction with a Dyonics@ light source and light cable, the 3252 DV Camera System is indicated for use in endoscopic surgical procedures in the thoracic cavity when used with an appropriately indicated thoracoscope.

Source page: https://510kreport.com/device/K031379
Methodology: https://510kreport.com/methodology