MAXIVIEW DIAGNOSTIC WORKSTATION— 510(k) K930500

Name: FDA 510(k) clearance K930500
Creator: U.S. Food and Drug Administration
Published: 1993-12-29

Substantially Equivalent

Dimensional Medicine, Inc.

FDA 510(k) clearance K930500 for MAXIVIEW DIAGNOSTIC WORKSTATION, Substantially Equivalent on 1993-12-29. Applicant: Dimensional Medicine, Inc.. Device class: 1.

Clearance details

Applicant: Dimensional Medicine, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1993-02-01
Decision date: 1993-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minnetonka, MN, US

Download summary PDF View on FDA.gov ↗

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