VISIONLINK INTERFILE CONVERSION SOFTWARE— 510(k) K933372

Name: FDA 510(k) clearance K933372
Creator: U.S. Food and Drug Administration
Published: 1993-11-01

Substantially Equivalent

Evergreen Technologies, Inc.

FDA 510(k) clearance K933372 for VISIONLINK INTERFILE CONVERSION SOFTWARE, Substantially Equivalent on 1993-11-01. Applicant: Evergreen Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Evergreen Technologies, Inc.
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 1993-07-09
Decision date: 1993-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Castine, ME, US

Download summary PDF View on FDA.gov ↗

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K935103 — VISIONLINK ACR-NEMA CONVERSION UTILITIES1994-02-09
K933209 — VISIONTOOL1993-09-29
K924178 — MEDVISION(TM) IMAGING SOFTWARE1993-02-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.