MEDVISION ENVIROMENT/MEDVISION 2.0— 510(k) K942861

Name: FDA 510(k) clearance K942861
Creator: U.S. Food and Drug Administration
Published: 1994-12-07

Substantially Equivalent

Evergreen Technologies, Inc.

FDA 510(k) clearance K942861 for MEDVISION ENVIROMENT/MEDVISION 2.0, Substantially Equivalent on 1994-12-07. 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: 1994-06-17
Decision date: 1994-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Castine, ME, US

Download summary PDF View on FDA.gov ↗

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