IMAGE TRANSPORT SERIES III— 510(k) K925964

Name: FDA 510(k) clearance K925964
Creator: U.S. Food and Drug Administration
Published: 1995-02-03

Substantially Equivalent

Dataview Imaging Intl., Inc.

FDA 510(k) clearance K925964 for IMAGE TRANSPORT SERIES III, Substantially Equivalent on 1995-02-03. Applicant: Dataview Imaging Intl., Inc.. Device class: 1.

Clearance details

Applicant: Dataview Imaging Intl., Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1992-11-25
Decision date: 1995-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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