# K953974: Camvision 1000

- Pathway: 510(k) (Traditional)
- Applicant: Medivision Medical Imaging, Ltd.
- Decided: Sep 9, 1996 after 383 days
- Product code: JAA (System, X-Ray, Fluoroscopic, Image-Intensified)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K990066: CCD Camera, Model 9000 (1999), 4 descendants of its own
- K162268: Senographe Pristina (2016), 3 descendants of its own
- K211725: Senographe Pristina (2021), 1 descendant of its own
- K260087: Senographe Pristina; SenoBright HD; Pristina Serena; Pristina Serena Bright (2026), 0 descendants of its own
- K163302: Senographe Pristina (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K953974
Methodology: https://510kreport.com/methodology