EURAMARK 610 PHOTOMETER— 510(k) K903164

Name: FDA 510(k) clearance K903164
Creator: U.S. Food and Drug Administration
Published: 1990-08-09

Substantially Equivalent

Euro-American Marketing Group, Inc.

FDA 510(k) clearance K903164 for EURAMARK 610 PHOTOMETER, Substantially Equivalent on 1990-08-09. Applicant: Euro-American Marketing Group, Inc.. Device class: 1.

Clearance details

Applicant: Euro-American Marketing Group, Inc.
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1990-07-18
Decision date: 1990-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mount Prospect, IL, US

Download summary PDF View on FDA.gov ↗

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