510(k) Report

510(k) · Cleared

Cleared

Maxiview Diagnostic Workstation

K930500510(k) TraditionalCleared Dec 29, 1993331-day reviewClass I21 CFR 892.2020

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Dimensional Medicine, Inc. · LMD System, Digital Image Communications, Radiological

Cleared on Dec 29, 1993 after a 331-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided
Dec 29, 1993
Review
331 days
Class
Class I
Product code
LMD
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared1990200020102020
  1. This deviceK930500 Maxiview Diagnostic WorkstationDimensional Medicine, Inc. · 1993
  2. Descendant · cites it directly · 0 of its ownK984023 Maxview Diagnostic WorkstationDynamic Healthcare Technologies, Inc. · 1998

Most influential descendants

Showing 1 of 1 · See all
  • K984023Maxview Diagnostic WorkstationDynamic Healthcare Technologies, Inc. · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K930500Maxiview Diagnostic WorkstationDimensional Medicine, Inc.1993—
+1K984023Maxview Diagnostic WorkstationDynamic Healthcare Technologies, Inc.1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
FIG. 1 — Lineage of K930500, 1993–1998Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K984023Maxview Diagnostic WorkstationDynamic Healthcare Technologies, Inc.19980

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K984023 (Dynamic Healthcare Technologies, Inc., 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LMD devices

LMD System, Digital Image Communications, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LMD

FDA has decided no LMD device since 2007.

Median 510(k) review, days · LMD

Too few LMD 510(k)s in any year since 2007 to give a median.

Recalls per year · LMD

2in 2020

2007: 22008: 12009: 12012: 12015: 12020: 2
2007high 2 (2007) · low 0 (2010)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LMD

16in 2025

2007: 12008: 22009: 32010: 92011: 12012: 22013: 42014: 122015: 92016: 32017: 22018: 42019: 22020: 22021: 22022: 62023: 72024: 82025: 16
2007high 16 (2025) · low 1 (2007)2025

MAUDE reports naming product code LMD, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—21
20080—12
20090—13
20100—09
20110—01
20120—12
20130—04
20140—012
20150—19
20160—03
20170—02
20180—04
20190—02
20200—22
20210—02
20220—06
20230—07
20240—08
20250—016
20260—0—

More from Dimensional Medicine, Inc.

4 FDA decisions under this applicant name. See the company

  • K932564RadstatDimensional Medicine, Inc. · 1994
  • K920851MacviewDimensional Medicine, Inc. · 1993
  • K844317Dmi ConsoleDimensional Medicine, Inc. · 1985

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https://510kreport.com/device/K930500 · printed Nov 3, 2026

Cite this page

510(k) Report. “K930500: Maxiview Diagnostic Workstation.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K930500

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026