# K243703: TechLive

- Pathway: 510(k) (Traditional)
- Applicant: DeepHealth, Inc.
- Decided: Jun 5, 2025 after 188 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: 7 generations back to K971684 (1997). 30 ancestors in all.
No later device cites it as a predicate yet.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K232744: syngo Virtual Cockpit (VB10A), Siemens Healthcare GmbH (2023) Summary page 6.

## Indications for use
TechLive is a software application intended to provide remote access for real-time image acquisition, assistance, review, monitoring and standardization of imaging devices across multiple locations. It is a vendor neutral solution allowing read-only or full access control to connected devices. TechLive is also intended for training of medical personnel working on medical imaging devices. TechLive is not intended for diagnostic use.

Source page: https://510kreport.com/device/K243703
Methodology: https://510kreport.com/methodology