MODEL 2730 CLINICAL REFRACTOMETER— 510(k) K941906

Name: FDA 510(k) clearance K941906
Creator: U.S. Food and Drug Administration
Published: 1995-01-17

Substantially Equivalent

Vee Gee Scientific, Inc.

FDA 510(k) clearance K941906 for MODEL 2730 CLINICAL REFRACTOMETER, Substantially Equivalent on 1995-01-17. Applicant: Vee Gee Scientific, Inc.. Device class: 1.

Clearance details

Applicant: Vee Gee Scientific, Inc.
Product code: Code JRE
Device class: Class 1
Regulation: 21 CFR 862.2800
Advisory panel: Clinical Chemistry
Date received: 1994-04-19
Decision date: 1995-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kirkland, WA, US

Download summary PDF View on FDA.gov ↗

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