# K130929: Zmed VP4000

- Pathway: 510(k) (Traditional)
- Applicant: Zmed, Inc.
- Decided: Apr 12, 2013 after 9 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- 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 K864584 (1986). 2 ancestors in all.
9 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962260: Real-Time Video Contrast Enhancer, Digivision, Inc. (1996) Summary page 1.

## Most influential descendants
- K201434: Connected OR Hub with Voice Control, Connected OR Hub with Device Control (2020), 8 descendants of its own
- K212055: Connected OR Hub with Device and Voice Control (2021), 6 descendants of its own
- K220108: SDC4K Information Management System with Device and Voice Control Package (2022), 5 descendants of its own
- K222079: Connected OR Hub with Device and Voice Control, SDC4K Information Management System with Device and Voice Control (2022), 4 descendants of its own
- K230886: Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control (2023), 3 descendants of its own

## Indications for use
The ZMED VP4000 Video Processor is intended for use in any application where a viewing device (fluoroscope. endloscope, laparoscope, etc.) and monitor are incorporated to aid in diagnosis and treatment of a disease such as an arthroscopy or cholecystectomy.

Source page: https://510kreport.com/device/K130929
Methodology: https://510kreport.com/methodology