MEDVISION(TM) IMAGING SOFTWARE— 510(k) K924178

Name: FDA 510(k) clearance K924178
Creator: U.S. Food and Drug Administration
Published: 1993-02-02

Substantially Equivalent

Evergreen Technologies, Inc.

FDA 510(k) clearance K924178 for MEDVISION(TM) IMAGING SOFTWARE, Substantially Equivalent on 1993-02-02. Applicant: Evergreen Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Evergreen Technologies, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1992-08-19
Decision date: 1993-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gaithersburg, MD, US

Download summary PDF View on FDA.gov ↗

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