# K930500: Maxiview Diagnostic Workstation

- Pathway: 510(k) (Traditional)
- Applicant: Dimensional Medicine, Inc.
- Decided: Dec 29, 1993 after 331 days
- Product code: LMD (System, Digital Image Communications, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K984023: Maxview Diagnostic Workstation (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K930500
Methodology: https://510kreport.com/methodology